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
A Sumatriptan Succinate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Sumatriptan Succinate, including repackagers and relabelers. The FDA regulates Sumatriptan Succinate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Sumatriptan Succinate 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 Sumatriptan Succinate supplier is an individual or a company that provides Sumatriptan Succinate active pharmaceutical ingredient (API) or Sumatriptan Succinate finished formulations upon request. The Sumatriptan Succinate suppliers may include Sumatriptan Succinate API manufacturers, exporters, distributors and traders.
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A Sumatriptan Succinate DMF (Drug Master File) is a document detailing the whole manufacturing process of Sumatriptan Succinate active pharmaceutical ingredient (API) in detail. Different forms of Sumatriptan Succinate DMFs exist exist since differing nations have different regulations, such as Sumatriptan Succinate USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Sumatriptan Succinate DMF submitted to regulatory agencies in the US is known as a USDMF. Sumatriptan Succinate USDMF includes data on Sumatriptan Succinate's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Sumatriptan Succinate USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Sumatriptan Succinate suppliers with USDMF on PharmaCompass.
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