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1. 1-(2-(dimethylamino)-1-(4-methoxyphenyl)ethyl)cyclohexanol Hcl
2. Cyclohexanol, 1-(2-(dimethylamino)-1-(4-methoxyphenyl)ethyl)-, Hydrochloride
3. Dobupal
4. Efexor
5. Effexor
6. Hydrochloride, Venlafaxine
7. Sila Venlafaxine
8. Sila-venlafaxine
9. Trevilor
10. Vandral
11. Venlafaxine
12. Wy 45,030
13. Wy 45030
14. Wy-45,030
15. Wy-45030
16. Wy45,030
17. Wy45030
1. 99300-78-4
2. Venlafaxine Hcl
3. Effexor
4. Efexor
5. Effexor Xr
6. Dobupal
7. Vandral
8. Venlafaxinehydrochloride
9. Wy-45030
10. Venlafaxine (hydrochloride)
11. Wy 45030
12. Wy-45,030
13. Wy 45030 Hydrochloride
14. 1-(2-(dimethylamino)-1-(4-methoxyphenyl)ethyl)cyclohexanol Hydrochloride
15. 1-[2-(dimethylamino)-1-(4-methoxyphenyl)ethyl]cyclohexanol Hydrochloride
16. Nsc-745751
17. 7d7rx5a8mo
18. Venlafaxine (as Hydrochloride)
19. 1-[2-(dimethylamino)-1-(4-methoxyphenyl)ethyl]cyclohexan-1-ol Hydrochloride
20. Cyclohexanol, 1-(2-(dimethylamino)-1-(4-methoxyphenyl)ethyl)-, Hydrochloride
21. 1-(2-(dimethylamino)-1-(4-methoxyphenyl)ethyl)cyclohexan-1-ol Hydrochloride
22. 1-[2-(dimethylamino)-1-(4-methoxyphenyl)ethyl]cyclohexan-1-ol;hydrochloride
23. Chebi:9944
24. Venlafaxine Hydrochloride [usan]
25. Venlafaxine Hydorchloride
26. Unii-7d7rx5a8mo
27. C17h27no2.hcl
28. Venlift
29. Vexor
30. D,l-venlafaxine, Hydrochloride
31. Venlafaxine Ea
32. Venlafaxine Xr
33. Effexor Lp
34. Effexor Xl
35. Efexor Xl
36. Venlafaxine, Hcl
37. Effexor (tn)
38. Venlafaxine Hydrochloride [usan:usp]
39. Venlafaxine Hydro Chloride
40. Dsstox_cid_27397
41. Dsstox_rid_82318
42. Dsstox_gsid_47397
43. Schembl41936
44. Mls001401454
45. Chembl1201066
46. Dtxsid8047397
47. Hy-b0196a
48. Bvf-012
49. Amy32694
50. Bcp21401
51. Dl-venlafaxine Hydrochloride- Bio-x
52. Tox21_302508
53. Tox21_500449
54. Nsc745751
55. S1441
56. Venlafaxine Hydrochloride (jan/usp)
57. Venlafaxine Hydrochloride [mi]
58. Akos000280874
59. Akos016340594
60. Ac-1696
61. Ccg-100979
62. Ccg-213270
63. H13v695
64. Ks-5049
65. Lp00449
66. Nc00229
67. Nsc 745751
68. Pw-4112
69. Venlafaxine Hydrochloride [jan]
70. Venlafaxine Hydrochloride [hsdb]
71. Ncgc00256703-01
72. Ncgc00261134-01
73. Venlafaxine Hydrochloride [mart.]
74. Venlafaxine Hydrochloride [vandf]
75. Bv164514
76. Smr000469154
77. Venlafaxine Hydrochloride [usp-rs]
78. Venlafaxine Hydrochloride [who-dd]
79. Cas-99300-78-4
80. Ft-0642395
81. Sw197609-3
82. V0110
83. Pf-00345408
84. D00821
85. Venlafaxine Hydrochloride [ep Impurity]
86. Venlafaxine Hydrochloride [ep Monograph]
87. Venlafaxine Hydrochloride [orange Book]
88. Venlafaxine Hydrochloride [usp Monograph]
89. A845995
90. Venlafaxine Hydrochloride, >=98% (hplc), Powder
91. Venlafaxine Hydrochloride 100 Microg/ml In Methanol
92. Q27108525
93. Venlafaxine Hydrochloride 100 Microg/ml In Acetonitrile
94. 1-[2-dimethylamino-1-(4-methoxyphenyl)ethyl]cyclohexanol -hcl
95. Venlafaxine Hydrochloride 1.0 Mg/ml In Methanol (as Free Base)
96. 1-[2-(dimethylamino)-1-(4-methoxyph Enyl)ethyl]cyclohexanol Hydrochloride
97. 1-[2-dimethylamino-1-(4-methoxy-phenyl)-ethyl]-cyclohexanol Hydrochloride
98. Venlafaxine Hydrochloride, European Pharmacopoeia (ep) Reference Standard
99. (+/-)-1-(.alpha.-((dimethylamino)methyl)-p-methoxybenzyl)cyclohexanol Hydrochloride
100. (rs)-1-(2-dimethylamino-1-(4-methoxyphenyl)ethyl)cyclohexanol Hydrochloride
101. 1-[2-(dimethylamino)-1-(4-methoxyphenyl)ethyl]-1-cyclohexanol Hydrochloride
102. Cyclohexanol, 1-[2-(dimethylamino)-1-(4-methoxyphenyl)ethyl]-, Hydrochloride (1:1
103. Venlafaxine For System Suitability, European Pharmacopoeia (ep) Reference Standard
104. Venlafaxine Hydrochloride, Pharmaceutical Secondary Standard; Certified Reference Material
105. Venlafaxine Hydrochloride, United States Pharmacopeia (usp) Reference Standard
106. Venlafaxine Hydrochloride Solution, 1.0 Mg/ml In Methanol (as Free Base), Ampule Of 1 Ml, Certified Reference Material
| Molecular Weight | 313.9 g/mol |
|---|---|
| Molecular Formula | C17H28ClNO2 |
| Hydrogen Bond Donor Count | 2 |
| Hydrogen Bond Acceptor Count | 3 |
| Rotatable Bond Count | 5 |
| Exact Mass | 313.1808568 g/mol |
| Monoisotopic Mass | 313.1808568 g/mol |
| Topological Polar Surface Area | 32.7 Ų |
| Heavy Atom Count | 21 |
| Formal Charge | 0 |
| Complexity | 279 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 1 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| Covalently Bonded Unit Count | 2 |
| 1 of 4 | |
|---|---|
| Drug Name | Effexor xr |
| Drug Label | Effexor XR is an extended-release capsule for oral administration that contains venlafaxine hydrochloride, a structurally novel antidepressant. It is designated (R/S)-1-[2-(dimethylamino)-1-(4-methoxyphenyl)ethyl] cyclohexanol hydrochloride or ()-1... |
| Active Ingredient | Venlafaxine hydrochloride |
| Dosage Form | Capsule, extended release |
| Route | Oral |
| Strength | eq 150mg base; eq 37.5mg base; eq 75mg base |
| Market Status | Prescription |
| Company | Wyeth Pharms |
| 2 of 4 | |
|---|---|
| Drug Name | Venlafaxine hydrochloride |
| PubMed Health | Venlafaxine (By mouth) |
| Drug Classes | Antidepressant |
| Drug Label | Venlafaxine hydrochloride extended-release capsules for oral administration contain venlafaxine hydrochloride, a structurally novel antidepressant. It is designated (R/S)-1-[2-(dimethylamino)-1-(4-methoxyphenyl)ethyl] cyclohexanol hydrochloride or (c... |
| Active Ingredient | Venlafaxine hydrochloride |
| Dosage Form | Tablet, extended release; Tablet; Capsule, extended release |
| Route | oral; Oral |
| Strength | 37.5mg; eq 100mg base; eq 225mg base; eq 50mg base; 150mg; eq 150mg base; eq 75mg base; 75mg; eq 25mg base; eq 37.5mg base |
| Market Status | Tentative Approval; Prescription |
| Company | Amneal Pharms; Wockhardt; Anchen Pharms; Teva; Alembic Pharms; Aurobindo Pharma; Sun Pharm Inds; Torrent Pharms; Osmotica Pharm; Sun Pharma Global; Vintage; Valeant Bermuda; Zydus Pharms Usa; Dr Reddys Labs; Orchid Hlthcare; Mylan; Impax Labs; Heritage Ph |
| 3 of 4 | |
|---|---|
| Drug Name | Effexor xr |
| Drug Label | Effexor XR is an extended-release capsule for oral administration that contains venlafaxine hydrochloride, a structurally novel antidepressant. It is designated (R/S)-1-[2-(dimethylamino)-1-(4-methoxyphenyl)ethyl] cyclohexanol hydrochloride or ()-1... |
| Active Ingredient | Venlafaxine hydrochloride |
| Dosage Form | Capsule, extended release |
| Route | Oral |
| Strength | eq 150mg base; eq 37.5mg base; eq 75mg base |
| Market Status | Prescription |
| Company | Wyeth Pharms |
| 4 of 4 | |
|---|---|
| Drug Name | Venlafaxine hydrochloride |
| PubMed Health | Venlafaxine (By mouth) |
| Drug Classes | Antidepressant |
| Drug Label | Venlafaxine hydrochloride extended-release capsules for oral administration contain venlafaxine hydrochloride, a structurally novel antidepressant. It is designated (R/S)-1-[2-(dimethylamino)-1-(4-methoxyphenyl)ethyl] cyclohexanol hydrochloride or (c... |
| Active Ingredient | Venlafaxine hydrochloride |
| Dosage Form | Tablet, extended release; Tablet; Capsule, extended release |
| Route | oral; Oral |
| Strength | 37.5mg; eq 100mg base; eq 225mg base; eq 50mg base; 150mg; eq 150mg base; eq 75mg base; 75mg; eq 25mg base; eq 37.5mg base |
| Market Status | Tentative Approval; Prescription |
| Company | Amneal Pharms; Wockhardt; Anchen Pharms; Teva; Alembic Pharms; Aurobindo Pharma; Sun Pharm Inds; Torrent Pharms; Osmotica Pharm; Sun Pharma Global; Vintage; Valeant Bermuda; Zydus Pharms Usa; Dr Reddys Labs; Orchid Hlthcare; Mylan; Impax Labs; Heritage Ph |
Antidepressive Agents, Second-Generation
A structurally and mechanistically diverse group of drugs that are not tricyclics or monoamine oxidase inhibitors. The most clinically important appear to act selectively on serotonergic systems, especially by inhibiting serotonin reuptake. (See all compounds classified as Antidepressive Agents, Second-Generation.)
Serotonin and Noradrenaline Reuptake Inhibitors
Drugs that selectively block or suppress the plasma membrane transport of SEROTONIN and NORADRENALINE into axon terminals and are used as ANTIDEPRESSIVE AGENTS. (See all compounds classified as Serotonin and Noradrenaline Reuptake Inhibitors.)
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Cohance Lifesciences, offers full range of CDMO services for small molecule APIs, intermediates, ADCs, Pellets and Formulations.
Date of Issue : 2022-07-07
Valid Till : 2025-07-21
Written Confirmation Number : WC-0150
Address of the Firm : APIUnit-l,R.SNo50/1,Mukteswarapuram Village, Jaggaiahpet Mandal, NTRDistrict-521...
Cohance Lifesciences, offers full range of CDMO services for small molecule APIs, intermediates, ADCs, Pellets and Formulations.
Venlafaxine Hydrochloride Ph. Eur
Date of Issue : 2022-07-07
Valid Till : 2025-07-21
Written Confirmation Number : WC-0150
Address of the Firm : APIUnit-l,R.SNo50/1,Mukteswarapuram Village, Jaggaiahpet Mandal, NTRDistrict-521...
Aarti Pharmalabs is a partner of choice for APIs & Intermediates and the largest Indian manufacturer of Xanthine Derivatives.
Venlafaxine Hydrochloride USP/Ph. Eur
Date of Issue : 2022-08-24
Valid Till : 2025-07-29
Written Confirmation Number : WC-0099
Address of the Firm : Plot No.E-50, 50/1 and 59/1, Unit ?IV, MIDC, Tarapur?401506, Taluka: Palghar, Di...
Venlafaxine Hydrochloride Ph. Eur
Date of Issue : 2022-07-26
Valid Till : 2025-07-02
Written Confirmation Number : WC-0081
Address of the Firm : API Division Panelav, Tal-Halol, Dist-Panchmahal, Gujarat, India
Venlafaxine Hydrochloride Ph. Eur
Date of Issue : 2022-06-17
Valid Till : 2025-02-07
Written Confirmation Number : WC-0082
Address of the Firm : Karakhadi Plot No. 842-843, At - Karakhdi, Tal. - Padra, Dist - Vadodara 391 450...
Venlafaxine Hydrochloride EP/USP/BP
Date of Issue : 2022-06-09
Valid Till : 2025-12-08
Written Confirmation Number : WC-0077
Address of the Firm : Block No. 422, ECP Canal Road Village - Luna, Tal - Padra, Dist - Vadodara GUjar...
Date of Issue : 2022-06-03
Valid Till : 2025-06-16
Written Confirmation Number : WC-0030n
Address of the Firm : UNIT-II, Annavaram (Post), Chippada Village, Bheemunipatnam Mandai, Visakhapatna...
Venlafaxine Hydrochloride USP/Ph. Eur
Date of Issue : 2022-06-08
Valid Till : 2025-07-02
Written Confirmation Number : WC-0091n
Address of the Firm : P.O. Sejavta, Dist. Ratlam, Madhya Pradesh, India.
VenlaFexine Hydrochloride USP/EP
Date of Issue : 2022-07-27
Valid Till : 2025-07-21
Written Confirmation Number : WC-0087
Address of the Firm : Plot No.1 to 5, 31 to 35 & 48 to 51, 26 & Kl201, Village Lakhmapur, Taluka Dindo...
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We are the TIEFENBACHER GROUP, Health Pioneers since 1963.
Regulatory Info : Registered in EU
Registration Country : Germany
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Dosage Form : Tablet
Dosage Strength : 25MG
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Regulatory Info : Registered in EU
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We are the TIEFENBACHER GROUP, Health Pioneers since 1963.
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Dosage Strength : 37.5MG
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Regulatory Info : Registered in EU
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We are the TIEFENBACHER GROUP, Health Pioneers since 1963.
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Dosage Form : Tablet
Dosage Strength : 50MG
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Regulatory Info : Registered in EU
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We are the TIEFENBACHER GROUP, Health Pioneers since 1963.
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Dosage Form : Tablet
Dosage Strength : 75MG
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Regulatory Info : Registered in EU
Registration Country : Germany
We are the TIEFENBACHER GROUP, Health Pioneers since 1963.
Regulatory Info : Registered in EU
Registration Country : Germany
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Dosage Form : SR Capsule
Dosage Strength : 37.5MG
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Regulatory Info : Registered in EU
Registration Country : Germany
We are the TIEFENBACHER GROUP, Health Pioneers since 1963.
Regulatory Info : Registered in EU
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Dosage Form : SR Capsule
Dosage Strength : 75MG
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Regulatory Info : Registered in EU
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We are the TIEFENBACHER GROUP, Health Pioneers since 1963.
Regulatory Info : Registered in EU
Registration Country : Germany
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Dosage Form : SR Capsule
Dosage Strength : 150MG
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Regulatory Info : Registered in EU
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Registration Country : Sweden
Brand Name : Efexor Depot
Dosage Form : DEPOTKAPSEL, HÅRD
Dosage Strength : 75 MG
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Brand Name : Venlafaxin Orifarm
Dosage Form : DEPOTKAPSEL, HÅRD
Dosage Strength : 150 MG
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Registration Country : Sweden
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DOSAGE - CAPSULE, EXTENDED RELEASE;ORAL - EQ ...DOSAGE - CAPSULE, EXTENDED RELEASE;ORAL - EQ 150MG BASE
USFDA APPLICATION NUMBER - 20699
DOSAGE - CAPSULE, EXTENDED RELEASE;ORAL - EQ ...DOSAGE - CAPSULE, EXTENDED RELEASE;ORAL - EQ 37.5MG BASE
USFDA APPLICATION NUMBER - 20699
DOSAGE - CAPSULE, EXTENDED RELEASE;ORAL - EQ ...DOSAGE - CAPSULE, EXTENDED RELEASE;ORAL - EQ 75MG BASE
USFDA APPLICATION NUMBER - 20699
DOSAGE - TABLET, EXTENDED RELEASE;ORAL - EQ 1...DOSAGE - TABLET, EXTENDED RELEASE;ORAL - EQ 150MG BASE
USFDA APPLICATION NUMBER - 22104
DOSAGE - TABLET, EXTENDED RELEASE;ORAL - EQ 2...DOSAGE - TABLET, EXTENDED RELEASE;ORAL - EQ 225MG BASE
USFDA APPLICATION NUMBER - 22104
DOSAGE - TABLET, EXTENDED RELEASE;ORAL - EQ 3...DOSAGE - TABLET, EXTENDED RELEASE;ORAL - EQ 37.5MG BASE
USFDA APPLICATION NUMBER - 22104
DOSAGE - TABLET, EXTENDED RELEASE;ORAL - EQ 7...DOSAGE - TABLET, EXTENDED RELEASE;ORAL - EQ 75MG BASE
USFDA APPLICATION NUMBER - 22104
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PharmaCompass offers a list of Venlafaxine 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 Venlafaxine Hydrochloride manufacturer or Venlafaxine Hydrochloride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Venlafaxine Hydrochloride manufacturer or Venlafaxine Hydrochloride supplier.
PharmaCompass also assists you with knowing the Venlafaxine Hydrochloride API Price utilized in the formulation of products. Venlafaxine Hydrochloride API Price is not always fixed or binding as the Venlafaxine Hydrochloride Price is obtained through a variety of data sources. The Venlafaxine Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Effexor hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Effexor hydrochloride, including repackagers and relabelers. The FDA regulates Effexor hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Effexor hydrochloride 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 Effexor hydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Effexor hydrochloride supplier is an individual or a company that provides Effexor hydrochloride active pharmaceutical ingredient (API) or Effexor hydrochloride finished formulations upon request. The Effexor hydrochloride suppliers may include Effexor hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Effexor hydrochloride suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Effexor hydrochloride DMF (Drug Master File) is a document detailing the whole manufacturing process of Effexor hydrochloride active pharmaceutical ingredient (API) in detail. Different forms of Effexor hydrochloride DMFs exist exist since differing nations have different regulations, such as Effexor hydrochloride USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Effexor hydrochloride DMF submitted to regulatory agencies in the US is known as a USDMF. Effexor hydrochloride USDMF includes data on Effexor hydrochloride's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Effexor hydrochloride USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Effexor hydrochloride 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 Effexor hydrochloride Drug Master File in Japan (Effexor hydrochloride JDMF) empowers Effexor hydrochloride 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 Effexor hydrochloride JDMF during the approval evaluation for pharmaceutical products. At the time of Effexor hydrochloride JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
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In Korea, the Ministry of Food and Drug Safety (MFDS) is in charge of regulating pharmaceutical products and services.
Pharmaceutical companies submit a Effexor hydrochloride Drug Master File in Korea (Effexor hydrochloride KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Effexor hydrochloride. The MFDS reviews the Effexor hydrochloride KDMF as part of the drug registration process and uses the information provided in the Effexor hydrochloride KDMF to evaluate the safety and efficacy of the drug.
After submitting a Effexor hydrochloride 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 Effexor hydrochloride API can apply through the Korea Drug Master File (KDMF).
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A Effexor hydrochloride CEP of the European Pharmacopoeia monograph is often referred to as a Effexor hydrochloride Certificate of Suitability (COS). The purpose of a Effexor hydrochloride CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Effexor hydrochloride EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Effexor hydrochloride to their clients by showing that a Effexor hydrochloride CEP has been issued for it. The manufacturer submits a Effexor hydrochloride CEP (COS) as part of the market authorization procedure, and it takes on the role of a Effexor hydrochloride CEP holder for the record. Additionally, the data presented in the Effexor hydrochloride CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Effexor hydrochloride DMF.
A Effexor hydrochloride CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Effexor hydrochloride CEPs may be accepted in nations that are not members of the Ph. Eur. at the discretion of the authorities there.
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A Effexor hydrochloride written confirmation (Effexor hydrochloride WC) is an official document issued by a regulatory agency to a Effexor hydrochloride manufacturer, verifying that the manufacturing facility of a Effexor hydrochloride active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Effexor hydrochloride APIs or Effexor hydrochloride finished pharmaceutical products to another nation, regulatory agencies frequently require a Effexor hydrochloride WC (written confirmation) as part of the regulatory process.
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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 Effexor hydrochloride as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Effexor hydrochloride 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 Effexor hydrochloride 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 Effexor hydrochloride and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Effexor hydrochloride NDC to their finished compounded human drug products, they may choose to do so.
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Effexor hydrochloride 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 Effexor hydrochloride 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 Effexor hydrochloride GMP manufacturer or Effexor hydrochloride GMP API supplier for your needs.
A Effexor hydrochloride CoA (Certificate of Analysis) is a formal document that attests to Effexor hydrochloride's compliance with Effexor hydrochloride specifications and serves as a tool for batch-level quality control.
Effexor hydrochloride CoA mostly includes findings from lab analyses of a specific batch. For each Effexor hydrochloride 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.
Effexor hydrochloride may be tested according to a variety of international standards, such as European Pharmacopoeia (Effexor hydrochloride EP), Effexor hydrochloride JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Effexor hydrochloride USP).
