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1. Akamin
2. Akne Puren
3. Akne-puren
4. Aknemin
5. Aknin Mino
6. Aknin-mino
7. Aknosan
8. Apo Minocycline
9. Apo-minocycline
10. Arestin
11. Blemix
12. Cyclomin
13. Cyclops
14. Dentomycin
15. Dynacin
16. Hydrochloride, Minocycline
17. Icht Oral
18. Icht-oral
19. Klinomycin
20. Lederderm
21. Mestacine
22. Minakne
23. Mino Wolff
24. Mino-wolff
25. Minocin
26. Minocin Mr
27. Minoclir
28. Minocycline
29. Minocycline Monohydrochloride
30. Minocycline, (4r-(4 Alpha,4a Beta,5a Beta,12a Beta))-isomer
31. Minolis
32. Minomycin
33. Minoplus
34. Minotab
35. Minox 50
36. Monohydrochloride, Minocycline
37. Mynocine
1. 13614-98-7
2. Minocycline Hcl
3. Arestin
4. Solodyn
5. Minomycin
6. Minocin
7. Dynacin
8. Periocline
9. Ximino
10. Minocycline (hydrochloride)
11. Vectrin
12. Minomax
13. (4s,4as,5ar,12as)-4,7-bis(dimethylamino)-3,10,12,12a-tetrahydroxy-1,11-dioxo-1,4,4a,5,5a,6,11,12a-octahydrotetracene-2-carboxamide Hydrochloride
14. Mynocine Hydrochloride
15. Minocycline (as Hydrochloride)
16. Minocycline, Hydrochloride
17. 4,7-bis(dimethylamino)-1,4,4a,5,5a,6,11,12a-octahydro-3,10,12,12a-tetrahydroxy-1,11-dioxo-2-naphthacenecarboxamide Monohydrochloride
18. 0020414e5u
19. Tri-mino
20. Nsc-141993
21. Dsstox_cid_24545
22. Dsstox_rid_80306
23. Dsstox_gsid_44545
24. (4s,4as,5ar,12ar)-4,7-bis(dimethylamino)-1,10,11,12a-tetrahydroxy-3,12-dioxo-4a,5,5a,6-tetrahydro-4h-tetracene-2-carboxamide;hydrochloride
25. [4s-(4alpha,4aalpha,5aalpha,12aalpha)]-4,7-bis(dimethylamino)-1,4,4a,5,5a,6,11,12a-octahydro-3,10,12,12a-tetrahydroxy-1,11-dioxonaphthacene-2-carboxamide Monohydrochloride
26. Lederderm
27. Mynocine
28. Acnez
29. Minomycin Chloride
30. Chebi:50697
31. (4s-(4alpha,4aalpha,5aalpha,12aalpha))-4,7-bis(dimethylamino)-1,4,4a,5,5a,6,11,12a-octahydro-3,10,12,12a-tetrahydroxy-1,11-dioxonaphthacene-2-carboxamide Monohydrochloride
32. [4s-(4?,4a?,5a?,12a?)]-4,7-bis(dimethylamino)-1,4,4a,5,5a,6,11,12a-octahydro-3,10,12,12a,tetrahydroxy-1,11-dioxo-2-naphthacenecarboxamide
33. 2-naphthacenecarboxamide, 4,7-bis(dimethylamino)-1,4,4a,5,5a,6,11,12a-octahydro-3,10,12,12a-tetrahydroxy-1,11-dioxo-, Hydrochloride (1:2), (4s,4as,5ar,12as)-
34. Einecs 237-099-7
35. Minocycline Hydrochloride (internal Use)
36. C23h27n3o7.hcl
37. Minocycline, Hcl
38. Unii-0020414e5u
39. Ncgc00096006-01
40. Prestwick_626
41. Arestin (tn)
42. Dynacin (tn)
43. Minocin (tn)
44. Solodyn (tn)
45. Minocycline Hydrochloride [usp:jan]
46. 7-dimethylamino-6-demethyl-6-deoxytetracycline, Hcl
47. Mfcd00083669
48. Minocyclinhydrochlorid
49. Amzeeq
50. Minolira
51. Zilxi
52. Minomycin Hydrochloride
53. Schembl2537
54. Cas-13614-98-7
55. 2-naphthacenecarboxamide, 4,7-bis(dimethylamino)-1,4,4a,5,5a,6,11,12a-octahydro-3,10,12,12a-tetrahydroxy-1,11-dioxo-, Monohydrochloride, (4s-(4alpha,4aalpha,5aalpha,12aalpha))-
56. Mls002548863
57. Spectrum1500414
58. Fxfm-244
59. Chembl1200881
60. Chembl4576719
61. Dtxsid8044545
62. Hms1568p12
63. Pharmakon1600-01500414
64. Bcp06597
65. Tox21_111250
66. Tox21_113183
67. Tox21_301590
68. Ccg-40107
69. Nsc757120
70. S4226
71. Minocycline Hydrochloride [mi]
72. Minocycline Hydrochloride, Crystalline
73. Akos015951312
74. Minocycline Hydrochloride (jp17/usp)
75. Tox21_111250_1
76. Cs-1256
77. Minocycline Hydrochloride [jan]
78. Nc00460
79. Nsc-757120
80. Minocycline Hydrochloride [mart.]
81. Minocycline Hydrochloride [vandf]
82. Ncgc00178854-03
83. Ncgc00255988-01
84. Ac-22362
85. As-75306
86. Hy-17412
87. Minocycline Hydrochloride [usp-rs]
88. Minocycline Hydrochloride [who-dd]
89. Smr001906766
90. M2288
91. D00850
92. Minocycline Hydrochloride [orange Book]
93. Minocycline Hydrochloride [usp Monograph]
94. 614m987
95. Sr-01000075625
96. Q-201407
97. Sr-01000075625-1
98. Q27104777
99. Minocycline Hydrochloride, Antibiotic For Culture Media Use Only
100. Minocycline Hydrochloride, European Pharmacopoeia (ep) Reference Standard
101. Minocycline Hydrochloride, Pharmaceutical Secondary Standard; Certified Reference Material
102. Minocycline Hydrochloride, United States Pharmacopeia (usp) Reference Standard
103. (4s,12as,4as,5ar)-4,7-bis(dimethylamino)-3,10,12,12a-tetrahydroxy-1,11-dioxo-4,5,6,12a,4a,5a-hexahydronaphthacene-2-carboxamide Hydrochloride
104. (4s,4as,5ar,12as)-4,7-bis(dimethylamino)-3,10,12,12a-tetrahydroxy-1,11-dioxo-1,4,4a,5,5a,6,11,12a-octahydrotetracene-2-carboxamidehydrochloride
105. 2-naphthacenecarboxamide, 4,7-bis(dimethylamino)-1,4,4a,5,5a,6,11,12a-octahydro-3,10,12,12a-tetrahydroxy-1,11-dioxo-, Monohydrochloride, (4s-(4.alpha.,4a.alpha.,5a.alpha.,12a.alpha.))-
| Molecular Weight | 493.9 g/mol |
|---|---|
| Molecular Formula | C23H28ClN3O7 |
| Hydrogen Bond Donor Count | 6 |
| Hydrogen Bond Acceptor Count | 9 |
| Rotatable Bond Count | 3 |
| Exact Mass | 493.1615779 g/mol |
| Monoisotopic Mass | 493.1615779 g/mol |
| Topological Polar Surface Area | 165 Ų |
| Heavy Atom Count | 34 |
| Formal Charge | 0 |
| Complexity | 971 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 4 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| Covalently Bonded Unit Count | 2 |
| 1 of 10 | |
|---|---|
| Drug Name | Arestin |
| PubMed Health | Minocycline |
| Drug Classes | Amebicide, Intestinal, Antiacne, Antiacne Antibacterial, Antibiotic, Antiprotozoal, Tetracycline |
| Drug Label | ARESTIN (minocycline hydrochloride) Microspheres is a subgingival sustained-release product containing the antibiotic minocycline hydrochloride incorporated into a bioresorbable polymer, Poly (glycolide-co-dl-lactide) or PGLA, for professional subg... |
| Active Ingredient | Minocycline hydrochloride |
| Dosage Form | Powder, extended release |
| Route | Dental |
| Strength | eq 1mg base |
| Market Status | Prescription |
| Company | Orapharma |
| 2 of 10 | |
|---|---|
| Drug Name | Dynacin |
| Drug Label | Minocycline hydrochloride, is a semisynthetic derivative of tetracycline, 4,7-Bis(dimethylamino)1,4,4a,5,5a,6,11,12a-octahydro-3,10,12,12a-tetrahydroxy-1, 11-dioxo-2naphthacenecarboxamide monohydrochloride. Its structural formula is:C23H27N3O7... |
| Active Ingredient | Minocycline hydrochloride |
| Dosage Form | Capsule |
| Route | Oral |
| Strength | eq 100mg base; eq 75mg base |
| Market Status | Prescription |
| Company | Cnty Line Pharms |
| 3 of 10 | |
|---|---|
| Drug Name | Minocin |
| PubMed Health | Minocycline, Regular Release (By mouth) |
| Drug Classes | Amebicide, Intestinal, Antiacne, Antibiotic, Antiprotozoal |
| Drug Label | MINOCIN minocycline hydrochloride, is a semisynthetic derivative of tetracycline, 4,7-Bis(dimethylamino)-1,4,4a,5,5a,6,11,12a-octahydro-3,10,12,12a-tetrahydroxy-1,11-dioxo-2-naphthacenecarboxamide monohydrochloride.Its structural formula is:C23H27N... |
| Active Ingredient | Minocycline hydrochloride |
| Dosage Form | Capsule; Injectable |
| Route | Injection; Oral |
| Strength | eq 100mg base; eq 50mg base; eq 100mg base/vial |
| Market Status | Prescription |
| Company | Rempex Pharms; Precision Dermat |
| 4 of 10 | |
|---|---|
| Drug Name | Minocycline hydrochloride |
| Drug Label | To reduce the development of drug-resistant bacteria and maintain the effectiveness of minocycline hydrochloride capsules and other antibacterial drugs, minocycline hydrochloride capsules should be used only to treat or prevent infections that are pr... |
| Active Ingredient | Minocycline hydrochloride |
| Dosage Form | Tablet, extended release; Tablet; Capsule |
| Route | oral; Oral |
| Strength | 65mg; 115mg; eq 100mg base; eq 50mg base; eq 105mg base; eq 65mg base; eq 115mg base; eq 75mg base; eq 90mg base; eq 80mg base; 55mg; eq 45mg base; eq 55mg base; eq 135mg base |
| Market Status | Tentative Approval; Prescription |
| Company | Mylan Pharms; Ranbaxy; Teva; Mylan Labs; Sun Pharm Inds; Aurobindo Pharma; Lupin; Barr Labs; Sandoz; Par Pharm; Watson Labs; Ranbaxy Labs; Dr Reddys Labs; Impax Labs |
| 5 of 10 | |
|---|---|
| Drug Name | Solodyn |
| PubMed Health | Minocycline |
| Drug Classes | Amebicide, Intestinal, Antiacne, Antiacne Antibacterial, Antibiotic, Antiprotozoal, Tetracycline |
| Drug Label | Minocycline hydrochloride, a semi synthetic derivative of tetracycline, is [4S-(4,4a,5a,12a)]-4,7-Bis(dimethylamino)-1,4,4a,5,5a,6,11,12a-octahydro-3,10,12,12a-tetrahydroxy-1,11-dioxo-2-naphthacenecarboxamide mono hydrochloride. The structura... |
| Active Ingredient | Minocycline hydrochloride |
| Dosage Form | Tablet, extended release |
| Route | Oral |
| Strength | eq 105mg base; eq 65mg base; eq 115mg base; eq 80mg base; eq 55mg base |
| Market Status | Prescription |
| Company | Medicis |
| 6 of 10 | |
|---|---|
| Drug Name | Arestin |
| PubMed Health | Minocycline |
| Drug Classes | Amebicide, Intestinal, Antiacne, Antiacne Antibacterial, Antibiotic, Antiprotozoal, Tetracycline |
| Drug Label | ARESTIN (minocycline hydrochloride) Microspheres is a subgingival sustained-release product containing the antibiotic minocycline hydrochloride incorporated into a bioresorbable polymer, Poly (glycolide-co-dl-lactide) or PGLA, for professional subg... |
| Active Ingredient | Minocycline hydrochloride |
| Dosage Form | Powder, extended release |
| Route | Dental |
| Strength | eq 1mg base |
| Market Status | Prescription |
| Company | Orapharma |
| 7 of 10 | |
|---|---|
| Drug Name | Dynacin |
| Drug Label | Minocycline hydrochloride, is a semisynthetic derivative of tetracycline, 4,7-Bis(dimethylamino)1,4,4a,5,5a,6,11,12a-octahydro-3,10,12,12a-tetrahydroxy-1, 11-dioxo-2naphthacenecarboxamide monohydrochloride. Its structural formula is:C23H27N3O7... |
| Active Ingredient | Minocycline hydrochloride |
| Dosage Form | Capsule |
| Route | Oral |
| Strength | eq 100mg base; eq 75mg base |
| Market Status | Prescription |
| Company | Cnty Line Pharms |
| 8 of 10 | |
|---|---|
| Drug Name | Minocin |
| PubMed Health | Minocycline, Regular Release (By mouth) |
| Drug Classes | Amebicide, Intestinal, Antiacne, Antibiotic, Antiprotozoal |
| Drug Label | MINOCIN minocycline hydrochloride, is a semisynthetic derivative of tetracycline, 4,7-Bis(dimethylamino)-1,4,4a,5,5a,6,11,12a-octahydro-3,10,12,12a-tetrahydroxy-1,11-dioxo-2-naphthacenecarboxamide monohydrochloride.Its structural formula is:C23H27N... |
| Active Ingredient | Minocycline hydrochloride |
| Dosage Form | Capsule; Injectable |
| Route | Injection; Oral |
| Strength | eq 100mg base; eq 50mg base; eq 100mg base/vial |
| Market Status | Prescription |
| Company | Rempex Pharms; Precision Dermat |
| 9 of 10 | |
|---|---|
| Drug Name | Minocycline hydrochloride |
| Drug Label | To reduce the development of drug-resistant bacteria and maintain the effectiveness of minocycline hydrochloride capsules and other antibacterial drugs, minocycline hydrochloride capsules should be used only to treat or prevent infections that are pr... |
| Active Ingredient | Minocycline hydrochloride |
| Dosage Form | Tablet, extended release; Tablet; Capsule |
| Route | oral; Oral |
| Strength | 65mg; 115mg; eq 100mg base; eq 50mg base; eq 105mg base; eq 65mg base; eq 115mg base; eq 75mg base; eq 90mg base; eq 80mg base; 55mg; eq 45mg base; eq 55mg base; eq 135mg base |
| Market Status | Tentative Approval; Prescription |
| Company | Mylan Pharms; Ranbaxy; Teva; Mylan Labs; Sun Pharm Inds; Aurobindo Pharma; Lupin; Barr Labs; Sandoz; Par Pharm; Watson Labs; Ranbaxy Labs; Dr Reddys Labs; Impax Labs |
| 10 of 10 | |
|---|---|
| Drug Name | Solodyn |
| PubMed Health | Minocycline |
| Drug Classes | Amebicide, Intestinal, Antiacne, Antiacne Antibacterial, Antibiotic, Antiprotozoal, Tetracycline |
| Drug Label | Minocycline hydrochloride, a semi synthetic derivative of tetracycline, is [4S-(4,4a,5a,12a)]-4,7-Bis(dimethylamino)-1,4,4a,5,5a,6,11,12a-octahydro-3,10,12,12a-tetrahydroxy-1,11-dioxo-2-naphthacenecarboxamide mono hydrochloride. The structura... |
| Active Ingredient | Minocycline hydrochloride |
| Dosage Form | Tablet, extended release |
| Route | Oral |
| Strength | eq 105mg base; eq 65mg base; eq 115mg base; eq 80mg base; eq 55mg base |
| Market Status | Prescription |
| Company | Medicis |
Anti-Bacterial Agents
Substances that inhibit the growth or reproduction of BACTERIA. (See all compounds classified as Anti-Bacterial Agents.)
GDUFA
DMF Review : Reviewed
Rev. Date : 2013-07-02
Pay. Date : 2013-06-20
DMF Number : 13758
Submission : 1998-09-01
Status : Active
Type : II
Certificate Number : R1-CEP 1999-002 - Rev 06
Issue Date : 2022-12-02
Type : Chemical
Substance Number : 1030
Status : Valid
Registration Number : 304MF10123
Registrant's Address : Rua da Estacao, 1 e 1A, 2600-726 Castanheira do Ribatejo, Portugal
Initial Date of Registration : 2022-08-17
Latest Date of Registration :
Registrant Name : Sam-O Pharmaceutical Co., Ltd.
Registration Date : 2024-01-31
Registration Number : 20240131-211-J-1572
Manufacturer Name : CIPAN - Companhia Industrial Produtora de Antibióticos, SA
Manufacturer Address : Rua da Estação, 1/1A, 2600-726 Castanheira do Ribatejo, Portugal
Curia - Accelerating therapies from discovery to commercialization with flexible, scalable CDMO solutions.
GDUFA
DMF Review : Reviewed
Rev. Date : 2013-01-30
Pay. Date : 2013-01-16
DMF Number : 14802
Submission : 2000-03-22
Status : Active
Type : II
Certificate Number : CEP 2000-107 - Rev 10
Issue Date : 2024-02-27
Type : Chemical
Substance Number : 1030
Status : Valid
Registration Number : 217MF10699
Registrant's Address : Via del Vecchio Politecnico n. 9, 20121 Milano (MI) - Italy
Initial Date of Registration : 2005-10-07
Latest Date of Registration :
NDC Package Code : 44657-0081
Start Marketing Date : 2019-10-31
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (30kg/30kg)
Marketing Category : BULK INGREDIENT
Capital Farma, a leading European pharmaceutical company focusing on the development & distribution of niche APIs & Pharma Services.
Curia - Accelerating therapies from discovery to commercialization with flexible, scalable CDMO solutions.
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 33279
Submission : 2018-11-28
Status : Active
Type : II
NDC Package Code : 44657-0051
Start Marketing Date : 2010-07-01
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (30kg/30kg)
Marketing Category : BULK INGREDIENT
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 26050
Submission : 2012-07-20
Status : Active
Type : II
NDC Package Code : 58623-0133
Start Marketing Date : 2019-09-04
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT

GDUFA
DMF Review : Reviewed
Rev. Date : 2019-05-10
Pay. Date : 2018-07-25
DMF Number : 32664
Submission : 2018-05-14
Status : Active
Type : II
Certificate Number : CEP 2022-195 - Rev 00
Issue Date : 2025-01-30
Type : Chemical
Substance Number : 1030
Status : Valid
NDC Package Code : 73402-112
Start Marketing Date : 2021-06-08
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Registrant Name : Ace Biopharm Co., Ltd.
Registration Date : 2022-09-05
Registration Number : 20220905-211-J-1355
Manufacturer Name : Zhejiang Changhai Pharmaceuticals Co.,Ltd.
Manufacturer Address : 188 Mid Zhiyuan Avenue, Binhai New Area, Shaoxing City, Zhejiang Province, 312366, PRChina

GDUFA
DMF Review : Reviewed
Rev. Date : 2022-07-25
Pay. Date : 2022-05-09
DMF Number : 35939
Submission : 2022-04-07
Status : Active
Type : II

GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 2408
Submission : 1975-02-26
Status : Inactive
Type : II

FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]
GDUFA
DMF Review : Complete
Rev. Date : 2013-07-02
Pay. Date : 2013-06-20
DMF Number : 13758
Submission : 1998-09-01
Status : Active
Type : II
Curia - Accelerating therapies from discovery to commercialization with flexible, scalable CDMO solutions.
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 33279
Submission : 2018-11-28
Status : Active
Type : II
Curia - Accelerating therapies from discovery to commercialization with flexible, scalable CDMO solutions.
GDUFA
DMF Review : Complete
Rev. Date : 2013-01-30
Pay. Date : 2013-01-16
DMF Number : 14802
Submission : 2000-03-22
Status : Active
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2013-01-15
Pay. Date : 2012-12-14
DMF Number : 13738
Submission : 1998-09-01
Status : Active
Type : II

GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 15014
Submission : 2000-10-02
Status : Active
Type : II

GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 13755
Submission : 1998-09-01
Status : Inactive
Type : II

GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 7849
Submission : 1989-01-04
Status : Inactive
Type : II

GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 13748
Submission : 1998-09-01
Status : Inactive
Type : II

GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 2408
Submission : 1975-02-26
Status : Inactive
Type : II

GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 13404
Submission : 1998-09-01
Status : Inactive
Type : II

FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Minocycline Hydrochloride Dihydrate
Certificate Number : R1-CEP 1999-002 - Rev 06
Status : Valid
Issue Date : 2022-12-02
Type : Chemical
Substance Number : 1030
Curia - Accelerating therapies from discovery to commercialization with flexible, scalable CDMO solutions.
Curia - Accelerating therapies from discovery to commercialization with flexible, scalable CDMO solutions.
Minocycline Hydrochloride Dihydrate
Certificate Number : CEP 2000-107 - Rev 10
Status : Valid
Issue Date : 2024-02-27
Type : Chemical
Substance Number : 1030
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Minocycline Hydrochloride Dihydrate, Grade B
Certificate Number : CEP 1997-078 - Rev 09
Status : Valid
Issue Date : 2024-07-17
Type : Chemical
Substance Number : 1030

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Minocycline Hydrochloride Dihydrate, Micronised
Certificate Number : R0-CEP 2022-299 - Rev 00
Status : Valid
Issue Date : 2022-10-11
Type : Chemical
Substance Number : 1030

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Minocycline Hydrochloride Dihydrate
Certificate Number : R0-CEP 1999-072 - Rev 02
Status : Withdrawn by Holder
Issue Date : 2004-08-20
Type : Chemical
Substance Number : 1030

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Minocycline Hydrochloride Dihydrate
Certificate Number : R1-CEP 1998-152 - Rev 02
Status : Valid
Issue Date : 2009-12-11
Type : Chemical
Substance Number : 1030

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Minocycline Hydrochloride Dihydrate
Certificate Number : CEP 2022-195 - Rev 00
Status : Valid
Issue Date : 2025-01-30
Type : Chemical
Substance Number : 1030

FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results] Registration Number : 304MF10123
Registrant's Address : Rua da Estacao, 1 e 1A, 2600-726 Castanheira do Ribatejo, Portugal
Initial Date of Registration : 2022-08-17
Latest Date of Registration : 2022-08-17
Curia - Accelerating therapies from discovery to commercialization with flexible, scalable CDMO solutions.
Registration Number : 217MF10699
Registrant's Address : Via del Vecchio Politecnico n. 9, 20121 Milano (MI) - Italy
Initial Date of Registration : 2005-10-07
Latest Date of Registration : 2020-01-31
Registration Number : 219MF10124
Registrant's Address : Sete Casas 2674-506 Loures PORTUGAL
Initial Date of Registration : 2007-04-18
Latest Date of Registration : 2017-12-06

FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Minocycline hydrochloride hydrate
Registrant Name : Sam-O Pharmaceutical Co., Ltd.
Registration Date : 2024-01-31
Registration Number : 20240131-211-J-1572
Manufacturer Name : CIPAN - Companhia Industrial...
Manufacturer Address : Rua da Estação, 1/1A, 2600-726 Castanheira do Ribatejo, Portugal
Registrant Name : Ace Biopharm Co., Ltd.
Registration Date : 2022-09-05
Registration Number : 20220905-211-J-1355
Manufacturer Name : Zhejiang Changhai Pharmaceut...
Manufacturer Address : 188 Mid Zhiyuan Avenue, Binhai New Area, Shaoxing City, Zhejiang Province, 312366, PR...

FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]About the Company : Suanfarma is a B2B life sciences company focused on developing, manufacturing, and distributing high-quality ingredients for the pharmaceutical industry in an innovative and sustai...
Curia - Accelerating therapies from discovery to commercialization with flexible, scalable CDMO solutions.
About the Company : Curia is a leading global CDMO with over 30 years of experience supporting clients across drug discovery, development, and commercial manufacturing. Leveraging deep scientific expe...
Capital Farma, a leading European pharmaceutical company focusing on the development & distribution of niche APIs & Pharma Services.
About the Company : Capital Farma provides integrated pharmaceutical solutions with a focus on high-quality Active Pharmaceutical Ingredients (APIs) sourced from leading European manufacturers. The co...
About the Company : Sumar Biotech LLP, registered in January 2018, is a startup approved by the Gujarat State Biotechnology Mission. Founded by young entrepreneurs and experienced research and manufac...
About the Company : Shamrock Pharmachemi Pvt Ltd. is a globally recognized API leader with 26+ years in human and veterinary pharmaceuticals. Operating in 40+ countries, it owns two Gujarat facilities...
About the Company : Guangzhou Tosun Pharmaceutical was founded in 1999, which mainly focuses on importation & exportation of Active Pharmaceutical Ingrediants, Chemical Raw Materials, Intermediate, Ex...

About the Company : Haorui, established in 1997, is a manufacturer and supplier of APIs, intermediates, veterinary and food additives. Meanwhile, it is assisting global pharmaceutical companies to get...

About the Company : Zhejiang Hisun Chemical Co., Ltd (hereafter called as ”Hisun Chemical), founded in 1998, is a state-holding enterprise invested by State Development & Investment Corporation(SDIC...

About the Company : Zhejiang Huida Biotech Co., Ltd. is located in Hangzhou, Zhejiang Province. It was established in 2020 and is a holding subsidiary of Huadong Medicine Co., Ltd. The company focu...

About the Company : Zhejiang Medicine Co., Ltd. is a large-scale joint-stock comprehensive pharmaceutical enterprise which was set up in May 1997. Being approved in August 1999 by the China Securities...

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Minocycline is a Other Small Molecule drug candidate, which is currently being evaluated in phase II clinical studies for the treatment of Rosacea.
Lead Product(s): Minocycline Hydrochloride,Inapplicable
Therapeutic Area: Dermatology Brand Name: Undisclosed
Study Phase: Phase IIProduct Type: Miscellaneous
Sponsor: Undisclosed
Deal Size: Inapplicable Upfront Cash: Inapplicable
Deal Type: Inapplicable November 14, 2017
Lead Product(s) : Minocycline Hydrochloride,Inapplicable
Therapeutic Area : Dermatology
Highest Development Status : Phase II
Partner/Sponsor/Collaborator : Undisclosed
Deal Size : Inapplicable
Deal Type : Inapplicable
Details : Minocycline is a Other Small Molecule drug candidate, which is currently being evaluated in phase II clinical studies for the treatment of Rosacea.
Product Name : Undisclosed
Product Type : Miscellaneous
Upfront Cash : Inapplicable
November 14, 2017
Details:
FXFM244 (Minocycline) is a small molecule drug, which is currently being evaluated in Phase I clinical studies for the treatment of papillomatosis, familial cutaneous.
Lead Product(s): Minocycline Hydrochloride,Inapplicable
Therapeutic Area: Infections and Infectious Diseases Brand Name: FXFM244
Study Phase: Phase IProduct Type: Antibiotic
Sponsor: Journey Medical Corporation
Deal Size: Inapplicable Upfront Cash: Inapplicable
Deal Type: Inapplicable March 10, 2026

Lead Product(s) : Minocycline Hydrochloride,Inapplicable
Therapeutic Area : Infections and Infectious Diseases
Highest Development Status : Phase I
Partner/Sponsor/Collaborator : Journey Medical Corporation
Deal Size : Inapplicable
Deal Type : Inapplicable
Details : FXFM244 (Minocycline) is a small molecule drug, which is currently being evaluated in Phase I clinical studies for the treatment of papillomatosis, familial cutaneous.
Product Name : FXFM244
Product Type : Antibiotic
Upfront Cash : Inapplicable
March 10, 2026

Details:
Arestin (Minocycline) is a small molecule drug candidate, which is currently being evaluated in Phase I clinical studies for the treatment of Periodontitis.
Lead Product(s): Minocycline Hydrochloride,Inapplicable
Therapeutic Area: Dental and Oral Health Brand Name: Arestin
Study Phase: Phase IProduct Type: Antibiotic
Sponsor: ORAPHARMA
Deal Size: Inapplicable Upfront Cash: Inapplicable
Deal Type: Inapplicable December 22, 2025

Lead Product(s) : Minocycline Hydrochloride,Inapplicable
Therapeutic Area : Dental and Oral Health
Highest Development Status : Phase I
Partner/Sponsor/Collaborator : ORAPHARMA
Deal Size : Inapplicable
Deal Type : Inapplicable
Effect of Arestin-Enhanced SRP on Periodontal and Glycemic Outcomes in Diabetics
Details : Arestin (Minocycline) is a small molecule drug candidate, which is currently being evaluated in Phase I clinical studies for the treatment of Periodontitis.
Product Name : Arestin
Product Type : Antibiotic
Upfront Cash : Inapplicable
December 22, 2025

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Elutia will leverage its proven drug-eluting biologics platform with a more concentrated focus on advancing NXT-41x, a biomatrix that directly addresses the root causes of reconstruction infections.
Lead Product(s): Rifampicin,Minocycline Hydrochloride
Therapeutic Area: Infections and Infectious Diseases Brand Name: EluPro
Study Phase: Approved FDFProduct Type: Antibiotic
Sponsor: Boston Scientific
Deal Size: $88.0 million Upfront Cash: $88.0 million
Deal Type: Divestment October 01, 2025

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Lead Product(s) : Rifampicin,Minocycline Hydrochloride
Therapeutic Area : Infections and Infectious Diseases
Highest Development Status : Approved FDF
Partner/Sponsor/Collaborator : Boston Scientific
Deal Size : $88.0 million
Deal Type : Divestment
Elutia Announces Closing of BioEnvelope Business Sale to Boston Scientific
Details : Elutia will leverage its proven drug-eluting biologics platform with a more concentrated focus on advancing NXT-41x, a biomatrix that directly addresses the root causes of reconstruction infections.
Product Name : EluPro
Product Type : Antibiotic
Upfront Cash : $88.0 million
October 01, 2025

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EluPro is designed to prevent post-operative complications, such as infections, in patients with cardiac implantable electronic devices (CIEDs) like pacemakers and defibrillators.
Lead Product(s): Rifampicin,Minocycline Hydrochloride
Therapeutic Area: Infections and Infectious Diseases Brand Name: EluPro
Study Phase: Approved FDFProduct Type: Antibiotic
Sponsor: Undisclosed
Deal Size: Inapplicable Upfront Cash: Inapplicable
Deal Type: Inapplicable January 14, 2025

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Lead Product(s) : Rifampicin,Minocycline Hydrochloride
Therapeutic Area : Infections and Infectious Diseases
Highest Development Status : Approved FDF
Partner/Sponsor/Collaborator : Undisclosed
Deal Size : Inapplicable
Deal Type : Inapplicable
Elutia Announces Full Launch of EluPro™ Following Strong Initial Demand
Details : EluPro is designed to prevent post-operative complications, such as infections, in patients with cardiac implantable electronic devices (CIEDs) like pacemakers and defibrillators.
Product Name : EluPro
Product Type : Antibiotic
Upfront Cash : Inapplicable
January 14, 2025

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The agreement aims to provide access to Elutia’s innovative EluPro Antibiotic Eluting BioEnvelope, embedded with rifampin and minocycline, to S3P’s extensive network of 993 acute care facilities.
Lead Product(s): Rifampicin,Minocycline Hydrochloride
Therapeutic Area: Infections and Infectious Diseases Brand Name: EluPro
Study Phase: Approved FDFProduct Type: Antibiotic
Sponsor: Vizient
Deal Size: Undisclosed Upfront Cash: Undisclosed
Deal Type: Agreement January 06, 2025

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Lead Product(s) : Rifampicin,Minocycline Hydrochloride
Therapeutic Area : Infections and Infectious Diseases
Highest Development Status : Approved FDF
Partner/Sponsor/Collaborator : Vizient
Deal Size : Undisclosed
Deal Type : Agreement
Elutia Announces EluPro™ GPO Agreement with Southern Strategic Sourcing Partners
Details : The agreement aims to provide access to Elutia’s innovative EluPro Antibiotic Eluting BioEnvelope, embedded with rifampin and minocycline, to S3P’s extensive network of 993 acute care facilities.
Product Name : EluPro
Product Type : Antibiotic
Upfront Cash : Undisclosed
January 06, 2025

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Mino-Lok (MLT) is a novel antibiotic lock therapy that combines minocycline with edetate disodium, which is investigated for the treatment of patients with catheter-related blood stream infections.
Lead Product(s): Minocycline Hydrochloride,Edetate Calcium Disodium,Ethanol
Therapeutic Area: Infections and Infectious Diseases Brand Name: Mino-Lok
Study Phase: Phase IIIProduct Type: Miscellaneous
Sponsor: Undisclosed
Deal Size: Inapplicable Upfront Cash: Inapplicable
Deal Type: Inapplicable November 25, 2024

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Lead Product(s) : Minocycline Hydrochloride,Edetate Calcium Disodium,Ethanol
Therapeutic Area : Infections and Infectious Diseases
Highest Development Status : Phase III
Partner/Sponsor/Collaborator : Undisclosed
Deal Size : Inapplicable
Deal Type : Inapplicable
Citius Holds FDA Type C Meeting On Phase 3 Mino-Lok® Pathway for Approval
Details : Mino-Lok (MLT) is a novel antibiotic lock therapy that combines minocycline with edetate disodium, which is investigated for the treatment of patients with catheter-related blood stream infections.
Product Name : Mino-Lok
Product Type : Miscellaneous
Upfront Cash : Inapplicable
November 25, 2024

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FDA has approved Emrosi (minocycline hydrochloride extended release capsules), formerly referred to as DFD-29, for the treatment of inflammatory lesions of rosacea in adults.
Lead Product(s): Minocycline Hydrochloride,Inapplicable
Therapeutic Area: Dermatology Brand Name: Undisclosed
Study Phase: Approved FDFProduct Type: Miscellaneous
Sponsor: Undisclosed
Deal Size: Inapplicable Upfront Cash: Inapplicable
Deal Type: Inapplicable November 04, 2024

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Lead Product(s) : Minocycline Hydrochloride,Inapplicable
Therapeutic Area : Dermatology
Highest Development Status : Approved FDF
Partner/Sponsor/Collaborator : Undisclosed
Deal Size : Inapplicable
Deal Type : Inapplicable
Journey Medical Announces FDA Approval of Emrosi™ for Rosacea
Details : FDA has approved Emrosi (minocycline hydrochloride extended release capsules), formerly referred to as DFD-29, for the treatment of inflammatory lesions of rosacea in adults.
Product Name : Undisclosed
Product Type : Miscellaneous
Upfront Cash : Inapplicable
November 04, 2024

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EluPro is designed to prevent post-operative complications, such as infections, in patients with cardiac implantable electronic devices (CIEDs) like pacemakers and defibrillators.
Lead Product(s): Rifampicin,Minocycline Hydrochloride
Therapeutic Area: Infections and Infectious Diseases Brand Name: EluPro
Study Phase: Approved FDFProduct Type: Antibiotic
Sponsor: Undisclosed
Deal Size: Inapplicable Upfront Cash: Inapplicable
Deal Type: Inapplicable September 05, 2024

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Lead Product(s) : Rifampicin,Minocycline Hydrochloride
Therapeutic Area : Infections and Infectious Diseases
Highest Development Status : Approved FDF
Partner/Sponsor/Collaborator : Undisclosed
Deal Size : Inapplicable
Deal Type : Inapplicable
Elutia Implants First EluPro™, a Drug-Eluting BioEnvelope for Cardiac Use
Details : EluPro is designed to prevent post-operative complications, such as infections, in patients with cardiac implantable electronic devices (CIEDs) like pacemakers and defibrillators.
Product Name : EluPro
Product Type : Antibiotic
Upfront Cash : Inapplicable
September 05, 2024

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The net proceeds will support the Company’s advancement of its drug-eluting biomatrix product EluPro (rifampin), the world’s first antibiotic-eluting BioEnvelope for Post-surgical Infections.
Lead Product(s): Rifampicin,Minocycline Hydrochloride
Therapeutic Area: Infections and Infectious Diseases Brand Name: EluPro
Study Phase: Approved FDFProduct Type: Antibiotic
Sponsor: Lake Street Capital Markets
Deal Size: $15.7 million Upfront Cash: Undisclosed
Deal Type: Private Placement August 01, 2024

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Lead Product(s) : Rifampicin,Minocycline Hydrochloride
Therapeutic Area : Infections and Infectious Diseases
Highest Development Status : Approved FDF
Partner/Sponsor/Collaborator : Lake Street Capital Markets
Deal Size : $15.7 million
Deal Type : Private Placement
Elutia Announces Full Exercise of Warrants Generating $15.7 Million in Gross Proceeds
Details : The net proceeds will support the Company’s advancement of its drug-eluting biomatrix product EluPro (rifampin), the world’s first antibiotic-eluting BioEnvelope for Post-surgical Infections.
Product Name : EluPro
Product Type : Antibiotic
Upfront Cash : Undisclosed
August 01, 2024

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Regulatory Info : Deregistered
Registration Country : Sweden
Minocycline Hydrochloride Dihydrate
Brand Name : Arrest
Dosage Form : Oral Powder
Dosage Strength :
Packaging :
Approval Date : 19-12-2002
Application Number : 2.00E+13
Regulatory Info : Deregistered
Registration Country : Sweden

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Regulatory Info : Authorised
Registration Country : Malta
Brand Name : Minaxen
Dosage Form : Hard Capsule
Dosage Strength : 50MG
Packaging :
Approval Date : 2006-08-29
Application Number :
Regulatory Info : Authorised
Registration Country : Malta

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Regulatory Info : Allowed
Registration Country : Switzerland
Brand Name : Minocin Acne
Dosage Form : Film Coated Tablet
Dosage Strength : 50mg
Packaging :
Approval Date : 10/12/1984
Application Number : 45465
Regulatory Info : Allowed
Registration Country : Switzerland

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Regulatory Info : Authorized
Registration Country : Spain
Brand Name : Minocin
Dosage Form : Hard Capsule
Dosage Strength : 100MG
Packaging :
Approval Date : 01-05-1973
Application Number : 51179
Regulatory Info : Authorized
Registration Country : Spain

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Regulatory Info : Withdrawn
Registration Country : Malta
Brand Name : Minocin Sa
Dosage Form : Modified-Release Hard Capsule
Dosage Strength : 100MG
Packaging :
Approval Date : 2006-12-19
Application Number :
Regulatory Info : Withdrawn
Registration Country : Malta

Regulatory Info :
Registration Country : Italy
Brand Name : Minocin
Dosage Form : Minocycline 100Mg 8 Joined' Oral Use
Dosage Strength : 8 cps 100 mg
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Italy

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Regulatory Info :
Registration Country : Italy
Brand Name : Minocin
Dosage Form :
Dosage Strength : 16 Cps 50 Mg
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Italy

Portfolio PDF
Product Web Link
Virtual Booth
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Regulatory Info : Authorised
Registration Country : Malta
Brand Name : Minocin Sa
Dosage Form : Modified-Release Hard Capsule
Dosage Strength : 100MG
Packaging :
Approval Date : 2021-12-15
Application Number :
Regulatory Info : Authorised
Registration Country : Malta

Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
Regulatory Info : Authorised
Registration Country : Malta
Brand Name : Cipancin
Dosage Form : Film Coated Tablet
Dosage Strength : 100MG
Packaging :
Approval Date : 2025-08-11
Application Number :
Regulatory Info : Authorised
Registration Country : Malta

Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
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Regulatory Info : PRESCRIPTION
Registration Country : Canada
MINOCYCLINE (MINOCYCLINE HYDROCHLORIDE)
Brand Name : MINOCYCLINE
Dosage Form : CAPSULE
Dosage Strength : 100MG
Packaging :
Approval Date :
Application Number : 2084104
Regulatory Info : PRESCRIPTION
Registration Country : Canada

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Regulatory Info : PRESCRIPTION
Registration Country : Canada
MINOCYCLINE (MINOCYCLINE HYDROCHLORIDE)
Brand Name : MINOCYCLINE
Dosage Form : CAPSULE
Dosage Strength : 50MG
Packaging : 100/250
Approval Date :
Application Number : 2084090
Regulatory Info : PRESCRIPTION
Registration Country : Canada

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Regulatory Info : PRESCRIPTION
Registration Country : Canada
MINOCYCLINE (MINOCYCLINE HYDROCHLORIDE)
Brand Name : ARESTIN MICROSPHERES
Dosage Form : POWDER (EXTENDED RELEASE)
Dosage Strength : 1MG/4MG
Packaging : 24X1MG
Approval Date :
Application Number : 2278219
Regulatory Info : PRESCRIPTION
Registration Country : Canada

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Regulatory Info : Prescription
Registration Country : Canada
Brand Name : PMS-MINOCYCLINE
Dosage Form : CAPSULE
Dosage Strength : 50MG
Packaging : 100/250
Approval Date :
Application Number :
Regulatory Info : Prescription
Registration Country : Canada

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Regulatory Info : Prescription
Registration Country : Canada
Brand Name : PMS-MINOCYCLINE
Dosage Form : CAPSULE
Dosage Strength : 100MG
Packaging : 100/250
Approval Date :
Application Number :
Regulatory Info : Prescription
Registration Country : Canada

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Regulatory Info : Prescription
Registration Country : Canada
Brand Name : PMS-MINOCYCLINE
Dosage Form : CAPSULE
Dosage Strength : 50MG
Packaging : 100
Approval Date :
Application Number :
Regulatory Info : Prescription
Registration Country : Canada

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Regulatory Info : Prescription
Registration Country : Canada
Brand Name : PMS-MINOCYCLINE
Dosage Form : CAPSULE
Dosage Strength : 100MG
Packaging : 100
Approval Date :
Application Number :
Regulatory Info : Prescription
Registration Country : Canada

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Regulatory Info :
Registration Country : Australia
Brand Name : Minomycin-50
Dosage Form : tablet
Dosage Strength : 50 mg
Packaging : 60
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Australia
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Regulatory Info :
Registration Country : Australia
Brand Name : Minomycin-50
Dosage Form : tablet
Dosage Strength : 50 mg
Packaging : 60
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Australia
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Regulatory Info :
Registration Country : Australia
Brand Name : Akamin 50
Dosage Form : tablet
Dosage Strength : 50 mg
Packaging : 60
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Australia

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Regulatory Info :
Registration Country : Australia
Brand Name : Akamin 50
Dosage Form : tablet
Dosage Strength : 50 mg
Packaging : 60
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Australia

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Regulatory Info : Generic
Registration Country : South Africa
Brand Name : Cyclimycin
Dosage Form : CAP
Dosage Strength : 50mg
Packaging : 60X1mg
Approval Date :
Application Number :
Regulatory Info : Generic
Registration Country : South Africa
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Regulatory Info : Generic
Registration Country : South Africa
Brand Name : Cyclimycin
Dosage Form : CAP
Dosage Strength : 100mg
Packaging : 100X1mg
Approval Date :
Application Number :
Regulatory Info : Generic
Registration Country : South Africa
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Regulatory Info : Generic
Registration Country : South Africa
Brand Name : Sandoz Minocycline
Dosage Form : TAB
Dosage Strength : 50mg
Packaging : 60X1mg
Approval Date :
Application Number :
Regulatory Info : Generic
Registration Country : South Africa

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Regulatory Info : Generic
Registration Country : South Africa
Brand Name : Sandoz Minocycline
Dosage Form : TAB
Dosage Strength : 50mg
Packaging : 100X1mg
Approval Date :
Application Number :
Regulatory Info : Generic
Registration Country : South Africa

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Regulatory Info : Generic
Registration Country : South Africa
Brand Name : Sandoz Minocycline
Dosage Form : TAB
Dosage Strength : 100mg
Packaging : 20X1mg
Approval Date :
Application Number :
Regulatory Info : Generic
Registration Country : South Africa

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Regulatory Info : Generic
Registration Country : South Africa
Brand Name : Minotabs 50
Dosage Form : TAB
Dosage Strength : 50mg
Packaging : 60X1mg
Approval Date :
Application Number :
Regulatory Info : Generic
Registration Country : South Africa

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Registration Country : India
Brand Name : Minocycline Hydrochlor...
Dosage Form : Tablet
Dosage Strength : 50MG
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : India
Packaging :
Regulatory Info :
Dosage : Tablet
Dosage Strength : 50MG
Brand Name : Minocycline Hydrochlor...
Approval Date :
Application Number :
Registration Country : India
Regulatory Info :
Registration Country : India
Brand Name : Minocycline Hydrochlor...
Dosage Form : Tablet
Dosage Strength : 75MG
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : India
Packaging :
Regulatory Info :
Dosage : Tablet
Dosage Strength : 75MG
Brand Name : Minocycline Hydrochlor...
Approval Date :
Application Number :
Registration Country : India
Regulatory Info :
Registration Country : India
Brand Name : Minocycline Hydrochlor...
Dosage Form : Tablet
Dosage Strength : 100MG
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : India
Packaging :
Regulatory Info :
Dosage : Tablet
Dosage Strength : 100MG
Brand Name : Minocycline Hydrochlor...
Approval Date :
Application Number :
Registration Country : India
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Regulatory Info :
Registration Country : India
Brand Name :
Dosage Form : ER Tablet
Dosage Strength : 55MG
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : India

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Packaging :
Regulatory Info :
Dosage : ER Tablet
Dosage Strength : 55MG
Brand Name :
Approval Date :
Application Number :
Registration Country : India

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Registration Country : India
Brand Name :
Dosage Form : ER Tablet
Dosage Strength : 105MG
Packaging :
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Regulatory Info :
Registration Country : India

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Regulatory Info :
Dosage : ER Tablet
Dosage Strength : 105MG
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Approval Date :
Application Number :
Registration Country : India

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Registration Country : India
Brand Name :
Dosage Form : ER Tablet
Dosage Strength : 115MG
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Application Number :
Regulatory Info :
Registration Country : India

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Dosage : ER Tablet
Dosage Strength : 115MG
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Registration Country : India

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Regulatory Info :
Registration Country : Russia
Brand Name : Minolexin
Dosage Form : Capsule
Dosage Strength : 50MG
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Russia

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Dosage : Capsule
Dosage Strength : 50MG
Brand Name : Minolexin
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Application Number :
Registration Country : Russia

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Registration Country : India
Brand Name :
Dosage Form : Vial
Dosage Strength : 100MG/5ML
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Regulatory Info :
Registration Country : India

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Dosage : Vial
Dosage Strength : 100MG/5ML
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Registration Country : India

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Registration Country : India
Brand Name :
Dosage Form : Injection
Dosage Strength : 100mg
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Registration Country : India

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Dosage : Injection
Dosage Strength : 100mg
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Registration Country : India

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Registration Country : India
Brand Name : Minocycline Hydrochlor...
Dosage Form : Capsules
Dosage Strength : 50mg
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : India

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Brand Name : Minocycline Hydrochlor...
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Application Number :
Registration Country : India

FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]DRUG PRODUCT COMPOSITIONS
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PharmaCompass offers a list of Minocycline Hydrochloride API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, and more, enabling you to easily find the right Minocycline Hydrochloride manufacturer or Minocycline Hydrochloride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Minocycline Hydrochloride manufacturer or Minocycline Hydrochloride supplier.
A Solodyn manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Solodyn, including repackagers and relabelers. The FDA regulates Solodyn manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Solodyn API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
click here to find a list of Solodyn manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Solodyn supplier is an individual or a company that provides Solodyn active pharmaceutical ingredient (API) or Solodyn finished formulations upon request. The Solodyn suppliers may include Solodyn API manufacturers, exporters, distributors and traders.
click here to find a list of Solodyn suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PharmaCompass.
A Solodyn DMF (Drug Master File) is a document detailing the whole manufacturing process of Solodyn active pharmaceutical ingredient (API) in detail. Different forms of Solodyn DMFs exist exist since differing nations have different regulations, such as Solodyn USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Solodyn DMF submitted to regulatory agencies in the US is known as a USDMF. Solodyn USDMF includes data on Solodyn's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Solodyn USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Solodyn suppliers with USDMF on PharmaCompass.
The Pharmaceuticals and Medical Devices Agency (PMDA) established the Japan Drug Master File (JDMF), also known as the Master File (MF), to permit Japanese and foreign manufacturers of drug substances, intermediates, excipients, raw materials, and packaging materials (‘Products’) to voluntarily register confidential information about the production and management of their products in Japan.
The Solodyn Drug Master File in Japan (Solodyn JDMF) empowers Solodyn API manufacturers to present comprehensive information (e.g., production methods, data, etc.) to the review authority, i.e., PMDA (Pharmaceuticals & Medical Devices Agency).
PMDA reviews the Solodyn JDMF during the approval evaluation for pharmaceutical products. At the time of Solodyn JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
click here to find a list of Solodyn suppliers with JDMF on PharmaCompass.
In Korea, the Ministry of Food and Drug Safety (MFDS) is in charge of regulating pharmaceutical products and services.
Pharmaceutical companies submit a Solodyn Drug Master File in Korea (Solodyn KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Solodyn. The MFDS reviews the Solodyn KDMF as part of the drug registration process and uses the information provided in the Solodyn KDMF to evaluate the safety and efficacy of the drug.
After submitting a Solodyn KDMF to the MFDS, the registered manufacturer can provide importers or distributors with the registration number without revealing confidential information to Korean business partners. Applicants seeking to register their Solodyn API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Solodyn suppliers with KDMF on PharmaCompass.
A Solodyn CEP of the European Pharmacopoeia monograph is often referred to as a Solodyn Certificate of Suitability (COS). The purpose of a Solodyn CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Solodyn EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Solodyn to their clients by showing that a Solodyn CEP has been issued for it. The manufacturer submits a Solodyn CEP (COS) as part of the market authorization procedure, and it takes on the role of a Solodyn CEP holder for the record. Additionally, the data presented in the Solodyn CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Solodyn DMF.
A Solodyn CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Solodyn CEPs may be accepted in nations that are not members of the Ph. Eur. at the discretion of the authorities there.
click here to find a list of Solodyn suppliers with CEP (COS) on PharmaCompass.
National Drug Code is a comprehensive database maintained by the FDA that contains information on all drugs marketed in the US. This directory includes information about finished drug products, unfinished drug products, and compounded drug products, including those containing Solodyn as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Solodyn API and other APIs are published in this directory by the FDA.
The NDC unfinished drugs database includes product listing information submitted for all unfinished drugs, such as active pharmaceutical ingredients (APIs), drugs intended for further processing and bulk drug substances for compounding.
Pharmaceutical companies that manufacture Solodyn as an active pharmaceutical ingredient (API) must furnish the FDA with an updated record of all drugs that they produce, prepare, propagate, compound, or process for commercial distribution in the US at their facilities.
The NDC directory also contains data on finished compounded human drug products that contain Solodyn and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Solodyn NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Solodyn suppliers with NDC on PharmaCompass.
Solodyn Active pharmaceutical ingredient (API) is produced in GMP-certified manufacturing facility.
GMP stands for Good Manufacturing Practices, which is a system used in the pharmaceutical industry to make sure that goods are regularly produced and monitored in accordance with quality standards. The FDA’s current Good Manufacturing Practices requirements are referred to as cGMP or current GMP which indicates that the company follows the most recent GMP specifications. The World Health Organization (WHO) has its own set of GMP guidelines, called the WHO GMP. Different countries can also set their own guidelines for GMP like China (Chinese GMP) or the EU (EU GMP).
PharmaCompass offers a list of Solodyn GMP manufacturers, exporters & distributors, which can be sorted by USDMF, JDMF, KDMF, CEP (COS), WC, and more, enabling you to easily find the right Solodyn GMP manufacturer or Solodyn GMP API supplier for your needs.
A Solodyn CoA (Certificate of Analysis) is a formal document that attests to Solodyn's compliance with Solodyn specifications and serves as a tool for batch-level quality control.
Solodyn CoA mostly includes findings from lab analyses of a specific batch. For each Solodyn CoA document that a company creates, the USFDA specifies specific requirements, such as supplier information, material identification, transportation data, evidence of conformity and signature data.
Solodyn may be tested according to a variety of international standards, such as European Pharmacopoeia (Solodyn EP), Solodyn JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Solodyn USP).