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 1Alembic Pharmaceuticals Limited
04 1Alivus Life Sciences
05 1Aurobindo Pharma Limited
06 1Cadila Pharmaceuticals
07 1Chemeca Drugs
08 2Chemi SpA
09 1Cilag AG
10 1Derivados Quimicos SAU
11 1Dipharma
12 1Divis Laboratories
13 1Emnar Pharma
14 1Erregierre SpA
15 1HANZHONG HANJIANG VENTUREPHARM PHARMACEUTICAL LTD
16 2Hetero Drugs
17 2Hikal
18 1Ipca Laboratories
19 1Jubilant Generics
20 1Lupin Ltd
21 1NORDIC SYNTHESIS AB
22 1Olon S.p.A
23 1Seven Star Pharmaceutical
24 1Sifavitor srl
25 1Solmag
26 1Sun Pharmaceutical Industries Limited
27 1ZHEJIANG LANGHUA PHARMACEUTICAL
28 1Zhejiang Apeloa Jiayuan Pharmaceutical
29 1Zhejiang Shaxing Pharm. & Chem
30 2Zhejiang Supor Pharmaceuticals Co., LTD
31 2Zydus Lifesciences
32 1Blank
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
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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 Quomen manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Quomen, including repackagers and relabelers. The FDA regulates Quomen manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Quomen 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 Quomen supplier is an individual or a company that provides Quomen active pharmaceutical ingredient (API) or Quomen finished formulations upon request. The Quomen suppliers may include Quomen API manufacturers, exporters, distributors and traders.
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A Quomen DMF (Drug Master File) is a document detailing the whole manufacturing process of Quomen active pharmaceutical ingredient (API) in detail. Different forms of Quomen DMFs exist exist since differing nations have different regulations, such as Quomen USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Quomen DMF submitted to regulatory agencies in the US is known as a USDMF. Quomen USDMF includes data on Quomen's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Quomen USDMF is kept confidential to protect the manufacturer’s intellectual property.
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