Granules India Limited has high volume world-class facilities for APIs, PFIs, & FDFs, serving customers in over 80 countries.
01 1Granules India Limited
02 1Aarti Pharmalabs
03 1Supriya Lifescience
04 1Alembic Pharmaceuticals Limited
05 1Alivus Life Sciences
06 1Aurobindo Pharma Limited
07 1Cadila Pharmaceuticals
08 1Chemeca Drugs
09 2Chemi SpA
10 1Cilag AG
11 1Derivados Quimicos SAU
12 1Dipharma
13 1Divis Laboratories
14 1Emnar Pharma
15 1Erregierre SpA
16 1HANZHONG HANJIANG VENTUREPHARM PHARMACEUTICAL LTD
17 2Hetero Drugs
18 2Hikal
19 1Ipca Laboratories
20 1Jubilant Generics
21 1Lupin Ltd
22 1NORDIC SYNTHESIS AB
23 1Olon S.p.A
24 1Seven Star Pharmaceutical
25 1Sifavitor srl
26 1Solmag
27 1Sun Pharmaceutical Industries Limited
28 1ZHEJIANG LANGHUA PHARMACEUTICAL
29 1Zhejiang Apeloa Jiayuan Pharmaceutical
30 1Zhejiang Shaxing Pharm. & Chem
31 2Zhejiang Supor Pharmaceuticals Co., LTD
32 2Zydus Lifesciences
Granules India Limited has high volume world-class facilities for APIs, PFIs, & FDFs, serving customers in over 80 countries.
GDUFA
DMF Review : Complete
Rev. Date : 2021-05-27
Pay. Date : 2021-04-15
DMF Number : 35694
Submission : 2021-03-29
Status :
Type : II
Aarti Pharmalabs is a partner of choice for APIs & Intermediates and the largest Indian manufacturer of Xanthine Derivatives.
GDUFA
DMF Review : Complete
Rev. Date : 2013-10-19
Pay. Date : 2013-06-25
DMF Number : 27204
Submission : 2013-06-17
Status :
Type : II
Supriya Lifesciences is a cGMP-compliant API manufacturing organization with a leadership position across key & niche products.
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 33538
Submission : 2019-01-25
Status :
Type : II
22
PharmaCompass offers a list of Bupropion 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 Bupropion Hydrochloride manufacturer or Bupropion Hydrochloride supplier for your needs.
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A Wellbutrin SR manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Wellbutrin SR, including repackagers and relabelers. The FDA regulates Wellbutrin SR manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Wellbutrin SR API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A Wellbutrin SR supplier is an individual or a company that provides Wellbutrin SR active pharmaceutical ingredient (API) or Wellbutrin SR finished formulations upon request. The Wellbutrin SR suppliers may include Wellbutrin SR API manufacturers, exporters, distributors and traders.
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A Wellbutrin SR DMF (Drug Master File) is a document detailing the whole manufacturing process of Wellbutrin SR active pharmaceutical ingredient (API) in detail. Different forms of Wellbutrin SR DMFs exist exist since differing nations have different regulations, such as Wellbutrin SR USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Wellbutrin SR DMF submitted to regulatory agencies in the US is known as a USDMF. Wellbutrin SR USDMF includes data on Wellbutrin SR's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Wellbutrin SR USDMF is kept confidential to protect the manufacturer’s intellectual property.
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We have 32 companies offering Wellbutrin SR
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