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1. Anafranil
2. Chlomipramine
3. Chlorimipramine
4. Clomipramine
5. Clomipramine Maleate (1:1)
6. Clomipramine Monohydrochloride
7. Hydiphen
8. Hydrochloride, Clomipramine
9. Monohydrochloride, Clomipramine
1. 17321-77-6
2. Clomipramine Hcl
3. Anafranil
4. 3-(3-chloro-10,11-dihydro-5h-dibenzo[b,f]azepin-5-yl)-n,n-dimethylpropan-1-amine Hydrochloride
5. Chlorimipramine Hydrochloride
6. 3-chloroimipramine Hydrochloride
7. Chloroimipramine Monohydrochloride
8. Clomipramine (hydrochloride)
9. Clomipramine Monohydrochloride
10. 2lxw0l6gwj
11. Nsc-759323
12. G 34586
13. Mls000028511
14. Chebi:3755
15. G-34586
16. 3-chloro-5-(3-(dimethylamino)propyl)-10,11-dihydro-5h-dibenz(b,f)azepine Monohydrochloride
17. 5h-dibenz(b,f)azepine-5-propanamine, 3-chloro-10,11-dihydro-n,n-dimethyl-, Monohydrochloride
18. Anaphranil
19. Smr000058295
20. Anafranil (tn)
21. 3-(2-chloro-5,6-dihydrobenzo[b][1]benzazepin-11-yl)-n,n-dimethylpropan-1-amine;hydrochloride
22. (3-{5-chloro-2-azatricyclo[9.4.0.0^{3,8}]pentadeca-1(11),3(8),4,6,12,14-hexaen-2-yl}propyl)dimethylamine Hydrochloride
23. 3-(3-chloro-10,11-dihydro-5h-dibenzo[b,f]azepin-5-yl)-n,n-dimethylpropan-1-aminium Chloride
24. 5h-dibenz[b,f]azepine-5-propanamine, 3-chloro-10,11-dihydro-n,n-dimethyl-, Hydrochloride (1:1)
25. Anafranil Hydrochloride
26. Sr-01000003088
27. Einecs 241-344-3
28. Unii-2lxw0l6gwj
29. Cas-17321-77-6
30. Clomipramine, Hcl
31. Prestwick_72
32. Mfcd00069234
33. Vr-776
34. Cpd000058295
35. I615
36. Opera_id_368
37. Clomipramine Hydrochloride [usan:usp:jan]
38. Dsstox_cid_22633
39. Dsstox_rid_80064
40. Dsstox_gsid_42633
41. Schembl41747
42. Mls001074205
43. Mls002222159
44. Mls002548879
45. Spectrum2300061
46. Regid_for_cid_68539
47. Chembl1200710
48. Clomipramine-[d6] Hydrochloride
49. Dtxsid3042633
50. Clomipramine Hydrochloride- Bio-x
51. Hms1568f20
52. Pharmakon1600-02300061
53. Amy40405
54. Bcp28468
55. Hy-b0457
56. Tox21_301819
57. Tox21_500307
58. Ccg-39492
59. Nsc759323
60. S2541
61. Anafranil Hydrochloride; Chloripramine
62. Akos015895084
63. Clomipramine Hydrochloride (anafranil)
64. Ac-8082
65. Clomipramine Hydrochloride (jp17/usp)
66. Clomipramine Hydrochloride [mi]
67. Ks-1044
68. Lp00307
69. Nc00678
70. Nsc 759323
71. (non-labelled)clomipramine-13c-d3 Hcl
72. Clomipramine Hydrochloride [jan]
73. Clomipramine Hydrochloride [usan]
74. Ncgc00093756-01
75. Ncgc00093756-02
76. Ncgc00093756-03
77. Ncgc00093756-04
78. Ncgc00178275-01
79. Ncgc00178275-02
80. Ncgc00255897-01
81. Ncgc00260992-01
82. 5h-dibenz(b,f)azepine, 10,11-dihydro-3-chloro-5-(3-(dimethylamino)propyl)-, Monohydrochloride
83. Bc164325
84. Clomipramine Hydrochloride [mart.]
85. Clomipramine Hydrochloride [vandf]
86. Clomipramine Hydrochloride [usp-rs]
87. Clomipramine Hydrochloride [who-dd]
88. Eu-0100307
89. Ft-0623989
90. Sw196384-4
91. C 7291
92. Clomipramine Hydrochloride [green Book]
93. Clomipramine Hydrochloride [orange Book]
94. D00811
95. Mls-0090819.0001
96. Clomipramine Hydrochloride [ep Monograph]
97. 321c776
98. Clomipramine Hydrochloride [usp Monograph]
99. Clomipramine Hydrochloride, >=98% (hplc), Powder
100. Sr-01000003088-2
101. Sr-01000003088-4
102. Sr-01000003088-5
103. Sr-01000003088-9
104. Q27106187
105. Clomipramine Hydrochloride 1.0 Mg/ml In Methanol (as Free Base)
106. Clomipramine Hydrochloride, British Pharmacopoeia (bp) Reference Standard
107. 3-chloro-10,11-dihydro-n,n-dimethyl-5h-dibenz(z)[b,f]azepine-5-propanamine Hydrochloride
108. Clomipramine Hydrochloride, Pharmaceutical Secondary Standard; Certified Reference Material
109. Clomipramine Hydrochloride, United States Pharmacopeia (usp) Reference Standard
110. 3-(3-chloro-10,11-dihydro-5h-dibenzo[b,f]azepin-5-yl)-n,n-dimethylpropan-1-amine Hcl
111. Clomipramine Hydrochloride Solution, 1.0 Mg/ml In Methanol (as Free Base), Ampule Of 1 Ml, Certified Reference Material
112. Clomipramine Hydrochloride, For Microbiological Assay, European Pharmacopoeia (ep) Reference Standard
| Molecular Weight | 351.3 g/mol |
|---|---|
| Molecular Formula | C19H24Cl2N2 |
| Hydrogen Bond Donor Count | 1 |
| Hydrogen Bond Acceptor Count | 2 |
| Rotatable Bond Count | 4 |
| Exact Mass | 350.1316542 g/mol |
| Monoisotopic Mass | 350.1316542 g/mol |
| Topological Polar Surface Area | 6.5 Ų |
| Heavy Atom Count | 23 |
| Formal Charge | 0 |
| Complexity | 346 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| Covalently Bonded Unit Count | 2 |
| 1 of 4 | |
|---|---|
| Drug Name | Anafranil |
| PubMed Health | Clomipramine (By mouth) |
| Drug Classes | Antidepressant, Central Nervous System Agent |
| Drug Label | Anafranil (clomipramine hydrochloride) Capsules USP is an antiobsessional drug that belongs to the class (dibenzazepine) of pharmacologic agents known as tricyclic antidepressants. Anafranil is available as capsules of 25, 50, and 75 mg for oral a... |
| Active Ingredient | Clomipramine hydrochloride |
| Dosage Form | Capsule |
| Route | Oral |
| Strength | 75mg; 25mg; 50mg |
| Market Status | Prescription |
| Company | Mallinckrodt |
| 2 of 4 | |
|---|---|
| Drug Name | Clomipramine hydrochloride |
| Drug Label | Clomipramine hydrochloride capsules USP are an antiobsessional drug that belongs to the class (dibenzazepine) of pharmacologic agents known as tricyclic antidepressants. Clomipramine hydrochloride is available as capsules of 25, 50 and 75 mg for oral... |
| Active Ingredient | Clomipramine hydrochloride |
| Dosage Form | Capsule |
| Route | Oral |
| Strength | 75mg; 25mg; 50mg |
| Market Status | Prescription |
| Company | Teva; Taro; Sandoz; Mylan |
| 3 of 4 | |
|---|---|
| Drug Name | Anafranil |
| PubMed Health | Clomipramine (By mouth) |
| Drug Classes | Antidepressant, Central Nervous System Agent |
| Drug Label | Anafranil (clomipramine hydrochloride) Capsules USP is an antiobsessional drug that belongs to the class (dibenzazepine) of pharmacologic agents known as tricyclic antidepressants. Anafranil is available as capsules of 25, 50, and 75 mg for oral a... |
| Active Ingredient | Clomipramine hydrochloride |
| Dosage Form | Capsule |
| Route | Oral |
| Strength | 75mg; 25mg; 50mg |
| Market Status | Prescription |
| Company | Mallinckrodt |
| 4 of 4 | |
|---|---|
| Drug Name | Clomipramine hydrochloride |
| Drug Label | Clomipramine hydrochloride capsules USP are an antiobsessional drug that belongs to the class (dibenzazepine) of pharmacologic agents known as tricyclic antidepressants. Clomipramine hydrochloride is available as capsules of 25, 50 and 75 mg for oral... |
| Active Ingredient | Clomipramine hydrochloride |
| Dosage Form | Capsule |
| Route | Oral |
| Strength | 75mg; 25mg; 50mg |
| Market Status | Prescription |
| Company | Teva; Taro; Sandoz; Mylan |
As an aid in the treatment of separation related disorders in dogs manifested by destruction and inappropriate elimination (defecation and urination) and only in combination with behavioural modification techniques.
Antidepressive Agents, Tricyclic
Substances that contain a fused three-ring moiety and are used in the treatment of depression. These drugs block the uptake of norepinephrine and serotonin into axon terminals and may block some subtypes of serotonin, adrenergic, and histamine receptors. However, the mechanism of their antidepressant effects is not clear because the therapeutic effects usually take weeks to develop and may reflect compensatory changes in the central nervous system. (See all compounds classified as Antidepressive Agents, Tricyclic.)
Selective Serotonin Reuptake Inhibitors
Compounds that specifically inhibit the reuptake of serotonin in the brain. (See all compounds classified as Selective Serotonin Reuptake Inhibitors.)
QN06AA04
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DOSAGE - CAPSULE;ORAL - 25MG
USFDA APPLICATION NUMBER - 19906
DOSAGE - CAPSULE;ORAL - 50MG
USFDA APPLICATION NUMBER - 19906
DOSAGE - CAPSULE;ORAL - 75MG
USFDA APPLICATION NUMBER - 19906
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PharmaCompass offers a list of Clomipramine Hydrochloride 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 Clomipramine Hydrochloride manufacturer or Clomipramine Hydrochloride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Clomipramine Hydrochloride manufacturer or Clomipramine Hydrochloride supplier.
PharmaCompass also assists you with knowing the Clomipramine Hydrochloride API Price utilized in the formulation of products. Clomipramine Hydrochloride API Price is not always fixed or binding as the Clomipramine Hydrochloride Price is obtained through a variety of data sources. The Clomipramine Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A ANAFRANIL manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of ANAFRANIL, including repackagers and relabelers. The FDA regulates ANAFRANIL manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. ANAFRANIL 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 ANAFRANIL manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A ANAFRANIL supplier is an individual or a company that provides ANAFRANIL active pharmaceutical ingredient (API) or ANAFRANIL finished formulations upon request. The ANAFRANIL suppliers may include ANAFRANIL API manufacturers, exporters, distributors and traders.
click here to find a list of ANAFRANIL suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A ANAFRANIL DMF (Drug Master File) is a document detailing the whole manufacturing process of ANAFRANIL active pharmaceutical ingredient (API) in detail. Different forms of ANAFRANIL DMFs exist exist since differing nations have different regulations, such as ANAFRANIL USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A ANAFRANIL DMF submitted to regulatory agencies in the US is known as a USDMF. ANAFRANIL USDMF includes data on ANAFRANIL's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The ANAFRANIL USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of ANAFRANIL 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 ANAFRANIL Drug Master File in Japan (ANAFRANIL JDMF) empowers ANAFRANIL 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 ANAFRANIL JDMF during the approval evaluation for pharmaceutical products. At the time of ANAFRANIL 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 ANAFRANIL 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 ANAFRANIL Drug Master File in Korea (ANAFRANIL KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of ANAFRANIL. The MFDS reviews the ANAFRANIL KDMF as part of the drug registration process and uses the information provided in the ANAFRANIL KDMF to evaluate the safety and efficacy of the drug.
After submitting a ANAFRANIL 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 ANAFRANIL API can apply through the Korea Drug Master File (KDMF).
click here to find a list of ANAFRANIL suppliers with KDMF on PharmaCompass.
A ANAFRANIL CEP of the European Pharmacopoeia monograph is often referred to as a ANAFRANIL Certificate of Suitability (COS). The purpose of a ANAFRANIL CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of ANAFRANIL EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of ANAFRANIL to their clients by showing that a ANAFRANIL CEP has been issued for it. The manufacturer submits a ANAFRANIL CEP (COS) as part of the market authorization procedure, and it takes on the role of a ANAFRANIL CEP holder for the record. Additionally, the data presented in the ANAFRANIL CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the ANAFRANIL DMF.
A ANAFRANIL CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. ANAFRANIL 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 ANAFRANIL suppliers with CEP (COS) on PharmaCompass.
A ANAFRANIL written confirmation (ANAFRANIL WC) is an official document issued by a regulatory agency to a ANAFRANIL manufacturer, verifying that the manufacturing facility of a ANAFRANIL active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting ANAFRANIL APIs or ANAFRANIL finished pharmaceutical products to another nation, regulatory agencies frequently require a ANAFRANIL WC (written confirmation) as part of the regulatory process.
click here to find a list of ANAFRANIL suppliers with Written Confirmation (WC) 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 ANAFRANIL as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for ANAFRANIL 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 ANAFRANIL 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 ANAFRANIL and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a ANAFRANIL NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of ANAFRANIL suppliers with NDC on PharmaCompass.
ANAFRANIL 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 ANAFRANIL 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 ANAFRANIL GMP manufacturer or ANAFRANIL GMP API supplier for your needs.
A ANAFRANIL CoA (Certificate of Analysis) is a formal document that attests to ANAFRANIL's compliance with ANAFRANIL specifications and serves as a tool for batch-level quality control.
ANAFRANIL CoA mostly includes findings from lab analyses of a specific batch. For each ANAFRANIL 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.
ANAFRANIL may be tested according to a variety of international standards, such as European Pharmacopoeia (ANAFRANIL EP), ANAFRANIL JP (Japanese Pharmacopeia) and the US Pharmacopoeia (ANAFRANIL USP).
