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1. Chocola A
2. Retinol Palmitate
3. Retinyl Palmitate
1. Retinyl Palmitate
2. 79-81-2
3. Retinol Palmitate
4. Retinol, Hexadecanoate
5. All-trans-retinyl Palmitate
6. Arovit
7. Optovit-a
8. Retinyl Hexadecanoate
9. Aquapalm
10. Dispatabs Tabs
11. Vitazyme A
12. Optovit A
13. Axerophthol Palmitate
14. Trans-retinol Palmitate
15. Trans-retinyl Palmitate
16. [(2e,4e,6e,8e)-3,7-dimethyl-9-(2,6,6-trimethylcyclohexen-1-yl)nona-2,4,6,8-tetraenyl] Hexadecanoate
17. Lutavit A 500 Plus
18. All-trans-retinol Palmitate
19. Arovit (roche)
20. All-trans-vitamin A Palmitate
21. Aquasol A (tn)
22. Retinyl (vitamin A) Palmitate
23. Retinol Palmitate [jan]
24. O~15~-hexadecanoylretinol
25. Nsc-758478
26. 1d1k0n0vvc
27. Retinol, Palmitate, All-trans
28. Ester Found In Fish Liver Oils
29. Retinol Palmitate (6ci,7ci)
30. Chebi:17616
31. Palmitic Acid, Ester With Retinol
32. Retinol, Palmitate, All-trans- (8ci)
33. Ncgc00095056-03
34. Dsstox_cid_1241
35. Dsstox_rid_76033
36. Dsstox_gsid_21241
37. (2e,4e,6e,8e)-hexadecanoic Acid 3,7-dimethyl-9-(2,6,6-trimethyl-cyclohex-1-enyl)-nona-2, 4,6,8,tetraenyl Ester
38. Vitamin A Solubilized
39. Cas-79-81-2
40. (2e,4e,6e,8e)-3,7-dimethyl-9-(2,6,6-trimethylcyclohex-1-en-1-yl)nona-2,4,6,8-tetraen-1-yl Hexadecanoate
41. Smr000112463
42. Ccris 3280
43. Retinol, Palmitate, All-trans-
44. Einecs 201-228-5
45. Unii-1d1k0n0vvc
46. Brn 1917366
47. Retinylpalmitate
48. Retinol-palmitate
49. Retinyl-palmitate
50. Retinol, All-trans-, Palmitate
51. Palmitic Acid Retinol
52. Retinyl Palmitic Acid
53. Vitamin- A Palmitate
54. Retinyl Hexadecanoic Acid
55. Spectrum5_001201
56. All-(e)-retinol Palmitate
57. Bmse000501
58. Ec 201-228-5
59. Retinol Palmitate (jp17)
60. Chembl1675
61. Schembl41649
62. Mls001332437
63. Mls001332438
64. Spectrum1503604
65. All-trans-retinyl Hexadecanoate
66. Dtxsid1021241
67. Retinyl Palmitate [inci]
68. Hms500m11
69. Retinyl Palmitate [vandf]
70. Vitamin A Palmitate [mi]
71. Hms1922e10
72. Hms2093g13
73. Hms2268c06
74. Pharmakon1600-01503604
75. Retinol Palmitate [who-dd]
76. Retinyl Palmitate [usp-rs]
77. (2e,4e,6e,8e)-3,7-dimethyl-9-(2,6,6-trimethylcyclohex-1-en-1-yl)nona-2,4,6,8-tetraen-1-yl Palmitate
78. Amy13840
79. Hy-b1384
80. Vae 16:0
81. Vitamin A Palmitate [vandf]
82. Zinc8214494
83. Tox21_113452
84. Tox21_303008
85. Ccg-39342
86. Lmpr01090013
87. Mfcd00019414
88. Nsc758478
89. S4126
90. Retinol, O~15~-(1-oxohexadecyl)-
91. Akos015918435
92. Nsc 758478
93. Vitamin A Palmitate, 1.7 M.i.u./g
94. Idi1_000249
95. Ncgc00095056-01
96. Ncgc00095056-02
97. Ncgc00256427-01
98. Ac-20001
99. Vitamin A Palmitate [orange Book]
100. Sbi-0051830.p002
101. All-(e)-retinol Palmitate [who-ip]
102. Cs-0013116
103. C02588
104. C76552
105. D00164
106. Ab00052360_04
107. A839762
108. Sr-05000001910
109. Vitamin A Palmitate (solubilized) [vandf]
110. Q7316807
111. Sr-05000001910-1
112. Retinyl Palmitate (vitamin A Palmitate; Retinol Palmitate)
113. Retinyl Palmitate, Potency: >=1,700,000 Usp Units Per G
114. Vitamin A (as Palmitate & Beta Carotene) [vandf]
115. Retinyl Palmitate, Type Iv, ~1,800,000 Usp Units/g, Oil
116. Retinyl Palmitate, United States Pharmacopeia (usp) Reference Standard
117. [3,7-dimethyl-9-(2,6,6-trimethylcyclohexen-1-yl)nona-2,4,6,8-tetraenyl] Hexadecanoate
118. 3,7-dimethyl-9-(2,6,6,-trimethyl-1-cyclohexen-1-yl)-2,4,6,8-nonatetraen-1-ol Palmitate
119. (2e,4e,6e,8e)-3,7-dimethyl-9-(2,6,6-trimethyl-cyclohex-en-1-yl)-2,4,6,8-nonateetraen-1-yl-palmitate
120. (2e,4e,6e,8e)-3,7-dimethyl-9-(2,6,6-trimethylcyclohex-1-enyl)nona-2,4,6,8-tetraenyl Palmitate
121. 110067-62-4
122. Hexadecanoic Acid [(2e,4e,6e,8e)-3,7-dimethyl-9-(2,6,6-trimethyl-1-cyclohexenyl)nona-2,4,6,8-tetraenyl] Ester
123. Retinyl Palmitate (vitamin A Palmitate), Pharmaceutical Secondary Standard; Certified Reference Material
124. Retinyl Palmitate Solution, 100 Mug/ml (ethanol With 0.1% (w/v) Bht), Ampule Of 1 Ml, Certified Reference Material
| Molecular Weight | 524.9 g/mol |
|---|---|
| Molecular Formula | C36H60O2 |
| XLogP3 | 13.6 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 2 |
| Rotatable Bond Count | 21 |
| Exact Mass | 524.45933115 g/mol |
| Monoisotopic Mass | 524.45933115 g/mol |
| Topological Polar Surface Area | 26.3 Ų |
| Heavy Atom Count | 38 |
| Formal Charge | 0 |
| Complexity | 803 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 4 |
| Undefined Bond Stereocenter Count | 0 |
| Covalently Bonded Unit Count | 1 |
Anticarcinogenic Agents
Agents that reduce the frequency or rate of spontaneous or induced tumors independently of the mechanism involved. (See all compounds classified as Anticarcinogenic Agents.)
Antioxidants
Naturally occurring or synthetic substances that inhibit or retard oxidation reactions. They counteract the damaging effects of oxidation in animal tissues. (See all compounds classified as Antioxidants.)
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GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 17708
Submission : 2004-09-14
Status : Active
Type : II
GDUFA
DMF Review : Reviewed
Rev. Date : 2017-07-14
Pay. Date : 2017-01-10
DMF Number : 31038
Submission : 2016-10-28
Status : Active
Type : II
Registration Number : 219MF10114
Registrant's Address : Wurmisweg 576, CH-4303, Kaiseraugst, Switzerland
Initial Date of Registration : 2007-03-23
Latest Date of Registration :
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 6581
Submission : 1986-08-28
Status : Inactive
Type : II
Registration Number : 218MF10103
Registrant's Address : Wurmisweg 576, CH-4303, Kaiseraugst, Switzerland
Initial Date of Registration : 2006-01-30
Latest Date of Registration :
Registration Number : 222MF10268
Registrant's Address : 2-9-18 Misakicho, Chiyoda-ku, Tokyo
Initial Date of Registration : 2010-12-10
Latest Date of Registration :
Registration Number : 229MF10223
Registrant's Address : 2-9-18 Misakicho, Chiyoda-ku, Tokyo
Initial Date of Registration : 2017-12-25
Latest Date of Registration :
Registration Number : 217MF10450
Registrant's Address : 2-9-18 Misakicho, Chiyoda-ku, Tokyo
Initial Date of Registration : 2005-08-24
Latest Date of Registration :
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USDMF
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 6581
Submission : 1986-08-28
Status : Inactive
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2017-07-14
Pay. Date : 2017-01-10
DMF Number : 31038
Submission : 2016-10-28
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 17708
Submission : 2004-09-14
Status : Active
Type : II
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Regulatory Info :
Registration Country : Switzerland
Brand Name : Vitamin A Blache
Dosage Form : Eye Gel
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Regulatory Info :
Registration Country : Switzerland
Regulatory Info :
Registration Country : Italy
Brand Name : Vitalipid
Dosage Form : Retinol Palmitate+Ergocalciferolo+Alpha Tocopherol+Phytomenadione 69+1+0,64+20Mcg 10 Units Parenteral Use
Dosage Strength : BB 10 VIALS EV 10 ml
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Italy
Regulatory Info :
Registration Country : Italy
Brand Name : Vitalipid
Dosage Form : Retinol Palmitate+Ergocalciferolo+Alpha Tocopherol+Phytomenadione 99+0,5+0,91+15Mcg 10 Units Parenteral Use
Dosage Strength : AD 10 VIALS EV 10 ml
Packaging :
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Regulatory Info :
Registration Country : Italy
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DOSAGE - SOLUTION;INTRAVENOUS - 2 IU/ML;40MG/...DOSAGE - SOLUTION;INTRAVENOUS - 2 IU/ML;40MG/ML;12MCG/ML;40 IU/ML;1MCG/ML;3MG/ML;120MCG/ML;8MG/ML;1.2MG/ML;0.72MG/ML;1.2MG/ML;660 IU/ML;0.03MG/ML
USFDA APPLICATION NUMBER - 21163
DOSAGE - SOLUTION;INTRAVENOUS - 2 IU/ML;40MG/...DOSAGE - SOLUTION;INTRAVENOUS - 2 IU/ML;40MG/ML;12MCG/ML;40 IU/ML;1MCG/ML;3MG/ML;120MCG/ML;8MG/ML;1.2MG/ML;0.72MG/ML;1.2MG/ML;660 IU/ML;30MCG/ML
USFDA APPLICATION NUMBER - 21163
DOSAGE - INJECTABLE;INJECTION - EQ 50,000 UNI...DOSAGE - INJECTABLE;INJECTION - EQ 50,000 UNITS BASE/ML
USFDA APPLICATION NUMBER - 6823
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Dosage Form : Tablet
Grade : Not Available
Application : Fillers, Diluents & Binders
Excipient Details : It is used in producing the injection solution, reducing the encephalic pressure, the intraocular pressure etc.
Pharmacopoeia Ref : CP/BP/ EP/ USP/IP
Technical Specs : Pharma Grade/ Medicine Grade/Injectable Grade
Ingredient(s) : Mannitol
Dosage Form : Syrup
Grade : Not Available
Application : Taste Masking
Pharmacopoeia Ref : Not Available
Technical Specs : Pharma Grade/Food Grade
Ingredient(s) : Sorbitol
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ABOUT THIS PAGE
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PharmaCompass offers a list of Vitamin A Palmitate API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Vitamin A Palmitate manufacturer or Vitamin A Palmitate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Vitamin A Palmitate manufacturer or Vitamin A Palmitate supplier.
PharmaCompass also assists you with knowing the Vitamin A Palmitate API Price utilized in the formulation of products. Vitamin A Palmitate API Price is not always fixed or binding as the Vitamin A Palmitate Price is obtained through a variety of data sources. The Vitamin A Palmitate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Arovit manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Arovit, including repackagers and relabelers. The FDA regulates Arovit manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Arovit 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 Arovit manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Arovit supplier is an individual or a company that provides Arovit active pharmaceutical ingredient (API) or Arovit finished formulations upon request. The Arovit suppliers may include Arovit API manufacturers, exporters, distributors and traders.
click here to find a list of Arovit suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Arovit DMF (Drug Master File) is a document detailing the whole manufacturing process of Arovit active pharmaceutical ingredient (API) in detail. Different forms of Arovit DMFs exist exist since differing nations have different regulations, such as Arovit USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Arovit DMF submitted to regulatory agencies in the US is known as a USDMF. Arovit USDMF includes data on Arovit's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Arovit USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Arovit 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 Arovit Drug Master File in Japan (Arovit JDMF) empowers Arovit 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 Arovit JDMF during the approval evaluation for pharmaceutical products. At the time of Arovit 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 Arovit suppliers with JDMF on PharmaCompass.
Arovit 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 Arovit GMP manufacturers, exporters & distributors, which can be sorted by USDMF, JDMF, KDMF, CEP (COS), WC, API price, and more, enabling you to easily find the right Arovit GMP manufacturer or Arovit GMP API supplier for your needs.
A Arovit CoA (Certificate of Analysis) is a formal document that attests to Arovit's compliance with Arovit specifications and serves as a tool for batch-level quality control.
Arovit CoA mostly includes findings from lab analyses of a specific batch. For each Arovit 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.
Arovit may be tested according to a variety of international standards, such as European Pharmacopoeia (Arovit EP), Arovit JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Arovit USP).
