DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
01 1Dr.Reddy's Laboratories Limited
02 1Moehs Cantabra S.L
03 2Aarti Pharmalabs Limited
04 1AURORE PHARMACEUTICALS PRIVATE LIMITED
05 1Amoli Organics (A Division of Umedica Laboratories Pvt.Ltd.)
06 1Assia Chemical Industries Ltd - Teva Tech Site
07 2Cadila Pharmaceuticals Limited
08 1Chongqing Carelife Pharmaceutical Co., Ltd.
09 1Cipla Ltd.
10 1Divi's Laboratories Limited
11 1HIKAL LIMITED
12 1Hetero Drugs Limited
13 1Ipca Laboratories Limited
14 1MSN Life Sciences Private Limited
15 1Siegfried AG
16 1UQUIFA Mexico, S.A. DE C.V.
17 1Zhejiang Apeloa Jiayuan Pharmaceutical Co., Ltd.
18 1Zydus Lifesciences Limited
19 1zhejiang jiuzhou pharmaceutical Co., Ltd.
01 1AtoVenlafaxine Hydrochloride
02 2VENLAFAXINE HYDROCHLORIDE
03 1Venlafaxine HCL
04 2Venlafaxine HCl
05 12Venlafaxine Hydrochloride
06 1Venlafaxine Hydrochloride Polymorph B
07 1Venlafaxine Hydrochloride Polymorph C
08 1venlafaxine hydrochloride
01 3China
02 14India
03 1Israel
04 2Spain
05 1Switzerland
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
NDC Package Code : 55111-098
Start Marketing Date : 2005-05-11
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Moehs Group, a reference company in the production of pharmaceutical active ingredients.
NDC Package Code : 68069-0002
Start Marketing Date : 2009-10-28
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Aarti Pharmalabs is a partner of choice for APIs & Intermediates and the largest Indian manufacturer of Xanthine Derivatives.
NDC Package Code : 15308-1506
Start Marketing Date : 2012-12-14
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Aarti Pharmalabs is a partner of choice for APIs & Intermediates and the largest Indian manufacturer of Xanthine Derivatives.
NDC Package Code : 15308-2610
Start Marketing Date : 1998-01-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 58598-0012
Start Marketing Date : 2011-09-28
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 53104-7529
Start Marketing Date : 2016-01-01
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (25kg/25kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 57451-1207
Start Marketing Date : 2019-12-04
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 17205-567
Start Marketing Date : 2024-04-18
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 52286-0006
Start Marketing Date : 2009-11-05
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 12666-0004
Start Marketing Date : 2006-11-15
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
A Venlafaxine Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Venlafaxine Hydrochloride, including repackagers and relabelers. The FDA regulates Venlafaxine Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Venlafaxine 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 Venlafaxine Hydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Venlafaxine Hydrochloride supplier is an individual or a company that provides Venlafaxine Hydrochloride active pharmaceutical ingredient (API) or Venlafaxine Hydrochloride finished formulations upon request. The Venlafaxine Hydrochloride suppliers may include Venlafaxine Hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Venlafaxine Hydrochloride suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information 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 Venlafaxine Hydrochloride as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Venlafaxine 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 Venlafaxine 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 Venlafaxine Hydrochloride and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Venlafaxine Hydrochloride NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Venlafaxine Hydrochloride suppliers with NDC on PharmaCompass.
We have 19 companies offering Venlafaxine Hydrochloride
Get in contact with the supplier of your choice:
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