DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
01 2Dr. Reddy's Laboratories
02 2Moehs Iberica
03 1Apotex Pharmachem
04 1Asymchem Laboratories
05 2Aurobindo Pharma Limited
06 1Chromo Laboratories
07 1Cipla
08 1Divis Laboratories
09 1Hovione
10 2MSN Laboratories
11 3Natco Pharma
12 1Orchid Pharma
13 2Quimica Sintetica
14 4SMS Pharmaceuticals
15 1Sun Pharmaceutical Industries Limited
16 1Viatris
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 : 16534
Submission : 2003-03-21
Status :
Type : II
Moehs Group, a reference company in the production of pharmaceutical active ingredients.
GDUFA
DMF Review : Complete
Rev. Date : 2013-06-24
Pay. Date : 2013-06-19
DMF Number : 17352
Submission : 2004-04-29
Status :
Type : II
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
GDUFA
DMF Review : Complete
Rev. Date : 2024-12-17
Pay. Date : 2024-11-21
DMF Number : 37551
Submission : 2022-09-30
Status :
Type : II
Moehs Group, a reference company in the production of pharmaceutical active ingredients.
GDUFA
DMF Review : Complete
Rev. Date : 2013-11-22
Pay. Date : 2013-02-13
DMF Number : 24026
Submission : 2010-08-02
Status :
Type : II
100
PharmaCompass offers a list of Sumatriptan 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 Sumatriptan manufacturer or Sumatriptan supplier for your needs.
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A Frimig manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Frimig, including repackagers and relabelers. The FDA regulates Frimig manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Frimig 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 Frimig supplier is an individual or a company that provides Frimig active pharmaceutical ingredient (API) or Frimig finished formulations upon request. The Frimig suppliers may include Frimig API manufacturers, exporters, distributors and traders.
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A Frimig DMF (Drug Master File) is a document detailing the whole manufacturing process of Frimig active pharmaceutical ingredient (API) in detail. Different forms of Frimig DMFs exist exist since differing nations have different regulations, such as Frimig USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Frimig DMF submitted to regulatory agencies in the US is known as a USDMF. Frimig USDMF includes data on Frimig's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Frimig USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Frimig suppliers with USDMF on PharmaCompass.
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