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01 1Cohance Lifesciences

02 1Moehs Iberica

03 2Aarti Pharmalabs

04 2TAPI Technology & API Services

05 3Alembic Pharmaceuticals Limited

06 1Amino Chemicals

07 2Amoli Organics

08 1Apotex Pharmachem

09 1Atul Bioscience Ltd

10 2Cadila Pharmaceuticals

11 1Chongqing Carelife Pharmaceutical

12 1Cipla

13 1Divis Laboratories

14 1Gador SA

15 1Hetero Drugs

16 1Hikal

17 1Ind Swift Laboratories Limited

18 1Ipca Laboratories

19 1Lupin Ltd

20 1MSN Laboratories

21 1Megafine Pharma (P) Limited

22 1Orchid Pharma

23 1RANBAXY LABORATORIES LIMITED

24 2Siegfried AG

25 1Solara Active Pharma Sciences

26 1Sun Pharmaceutical Industries Limited

27 1Torrent Pharmaceuticals Limited

28 1UQUIFA

29 1Viatris

30 2Zhejiang Apeloa Jiayuan Pharmaceutical

31 2Zhejiang Jiuzhou Pharmaceutical

32 2Zydus Lifesciences

33 1Blank

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PharmaCompass

01

PharmaVenue
Not Confirmed
  • fda
  • EDQM
  • WHO-GMP

Virtual BoothCohance Lifesciences, offers full range of CDMO services for small molecule APIs, intermediates, ADCs, Pellets and Formulations.

GDUFA

DMF Review : Complete

Rev. Date : 2022-11-03

Pay. Date : 2022-10-12

DMF Number : 34507

Submission : 2020-01-11

Status : Active

Type : II

Cohance

02

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothMoehs Group, a reference company in the production of pharmaceutical active ingredients.

GDUFA

DMF Review : Complete

Rev. Date : 2013-04-10

Pay. Date : 2013-04-02

DMF Number : 17258

Submission : 2004-03-01

Status : Active

Type : II

Moehs Iberica

03

PharmaVenue
Not Confirmed
  • fda
  • EDQM
  • WHO-GMP

Virtual BoothAarti Pharmalabs is a partner of choice for APIs & Intermediates and the largest Indian manufacturer of Xanthine Derivatives.

GDUFA

DMF Review : Complete

Rev. Date : 2016-02-12

Pay. Date : 2016-01-28

DMF Number : 19879

Submission : 2006-10-11

Status : Active

Type : II

Aarti Industries Company Banner

04

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothTAPI offers customized CDMO Solutions for API development and manufacturing services.

GDUFA

DMF Review : Complete

Rev. Date : 2012-12-24

Pay. Date : 2012-11-13

DMF Number : 16281

Submission : 2002-12-02

Status : Active

Type : II

TAPI Company Banner

05

PharmaVenue
Not Confirmed
  • fda
  • EDQM
  • WHO-GMP

Virtual BoothAarti Pharmalabs is a partner of choice for APIs & Intermediates and the largest Indian manufacturer of Xanthine Derivatives.

GDUFA

DMF Review : Complete

Rev. Date : 2017-05-26

Pay. Date : 2015-07-13

DMF Number : 28433

Submission : 2014-07-28

Status : Active

Type : II

Aarti Industries Company Banner

06

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothTAPI offers customized CDMO Solutions for API development and manufacturing services.

GDUFA

DMF Review : N/A

Rev. Date :

Pay. Date :

DMF Number : 18983

Submission : 2005-11-28

Status : Inactive

Type : II

TAPI Company Banner

10

PharmaVenue
Not Confirmed

Venlafaxine Hydrochloride Manufacturers

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.

Venlafaxine Hydrochloride Suppliers

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.

Venlafaxine Hydrochloride USDMF

A Venlafaxine Hydrochloride DMF (Drug Master File) is a document detailing the whole manufacturing process of Venlafaxine Hydrochloride active pharmaceutical ingredient (API) in detail. Different forms of Venlafaxine Hydrochloride DMFs exist exist since differing nations have different regulations, such as Venlafaxine Hydrochloride USDMF, ASMF (EDMF), JDMF, CDMF, etc.

A Venlafaxine Hydrochloride DMF submitted to regulatory agencies in the US is known as a USDMF. Venlafaxine Hydrochloride USDMF includes data on Venlafaxine Hydrochloride's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Venlafaxine Hydrochloride USDMF is kept confidential to protect the manufacturer’s intellectual property.

click here to find a list of Venlafaxine Hydrochloride suppliers with USDMF on PharmaCompass.

Inform the supplier about your product requirements, specifying if you need a product with particular monograph like EP (Ph. Eur.), USP, JP, BP, or any other quality. In addition, clarify whether you need hydrochloride (HCl), anhydricum, base, micronisatum or a specific level of purity. To find reputable suppliers, utilize the filters and select those certified by GMP, FDA, or any other certification as per your requirement.
For your convenience, we have listed synonyms and CAS numbers to help you find the best supplier. The use of synonyms and CAS numbers can be helpful in identifying potential suppliers, but it is crucial to note that they might not always indicate the exact same product. It is important to confirm the product details with the supplier before making a purchase to ensure that it meets your requirements.