Metrochem has been delivering customized volume & quality products to customers across the world, taking utmost care of their needs.
01 1Metrochem API Private Limited
02 2Dr. Reddy's Laboratories
03 1Granules India Limited
04 2AstraZeneca
05 1Aurobindo Pharma Limited
06 1Chromo Laboratories
07 1Hetero Drugs
08 1Lupin Ltd
09 1Merck & Co
10 1Raks Pharma
11 1Shouguang Fukang Pharmaceutical Co., Ltd
12 2Sun Pharmaceutical Industries Limited
13 1Viatris
Metrochem has been delivering customized volume & quality products to customers across the world, taking utmost care of their needs.
GDUFA
DMF Review : Complete
Rev. Date : 2024-06-24
Pay. Date : 2024-05-23
DMF Number : 35390
Submission : 2020-11-20
Status :
Type : II
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 17706
Submission : 2004-09-24
Status :
Type : II
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 : 2021-11-12
Pay. Date : 2021-09-29
DMF Number : 31829
Submission : 2017-08-31
Status :
Type : II
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
GDUFA
DMF Review : Complete
Rev. Date : 2026-03-05
Pay. Date : 2026-02-02
DMF Number : 38882
Submission : 2023-09-29
Status :
Type : II
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PharmaCompass offers a list of Omeprazole Magnesium 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 Omeprazole Magnesium manufacturer or Omeprazole Magnesium supplier for your needs.
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A 95382-33-5 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of 95382-33-5, including repackagers and relabelers. The FDA regulates 95382-33-5 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. 95382-33-5 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 95382-33-5 supplier is an individual or a company that provides 95382-33-5 active pharmaceutical ingredient (API) or 95382-33-5 finished formulations upon request. The 95382-33-5 suppliers may include 95382-33-5 API manufacturers, exporters, distributors and traders.
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A 95382-33-5 DMF (Drug Master File) is a document detailing the whole manufacturing process of 95382-33-5 active pharmaceutical ingredient (API) in detail. Different forms of 95382-33-5 DMFs exist exist since differing nations have different regulations, such as 95382-33-5 USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A 95382-33-5 DMF submitted to regulatory agencies in the US is known as a USDMF. 95382-33-5 USDMF includes data on 95382-33-5's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The 95382-33-5 USDMF is kept confidential to protect the manufacturer’s intellectual property.
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We have 13 companies offering 95382-33-5
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