DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
01 1Dr. Reddy's Laboratories
02 2TAPI Technology & API Services
03 2Arch Pharmalabs
04 1Benzo Chem Industries Pvt
05 1Cipla
06 1Dishman Carbogen Amcis
07 2Emcure Pharmaceuticals
08 1Fresenius Kabi AB Brunna
09 1GLAND CHEMICALS PRIVATE LIMITED
10 2Hansoh Pharma
11 1Hetero Drugs
12 2Intas Pharmaceuticals
13 1Laurus Labs
14 1MSN Laboratories
15 1Olon S.p.A
16 1PharmaEssentia
17 1ScinoPharm Taiwan Ltd
18 2Shilpa Medicare
19 1Sun Pharmaceutical Industries Limited
20 1Viatris
21 1Yangtze River Pharmaceutical Group
22 1Zhejiang Hisun Pharmaceutical
23 1Zydus Lifesciences
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
GDUFA
DMF Review : Complete
Rev. Date : 2016-06-27
Pay. Date : 2016-06-06
DMF Number : 18857
Submission : 2005-10-11
Status :
Type : II
TAPI, a leading global supplier of APIs, provides over 350 products and customized CDMO solutions for every stage of development.
GDUFA
DMF Review : Complete
Rev. Date : 2012-12-20
Pay. Date : 2012-12-03
DMF Number : 20979
Submission : 2007-10-29
Status :
Type : II
TAPI, a leading global supplier of APIs, provides over 350 products and customized CDMO solutions for every stage of development.
GDUFA
DMF Review : Complete
Rev. Date : 2015-02-20
Pay. Date : 2013-08-20
DMF Number : 27402
Submission : 2014-02-20
Status :
Type : II
37
PharmaCompass offers a list of Gemcitabine 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 Gemcitabine manufacturer or Gemcitabine supplier for your needs.
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A 122111-03-9 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of 122111-03-9, including repackagers and relabelers. The FDA regulates 122111-03-9 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. 122111-03-9 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 122111-03-9 supplier is an individual or a company that provides 122111-03-9 active pharmaceutical ingredient (API) or 122111-03-9 finished formulations upon request. The 122111-03-9 suppliers may include 122111-03-9 API manufacturers, exporters, distributors and traders.
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A 122111-03-9 DMF (Drug Master File) is a document detailing the whole manufacturing process of 122111-03-9 active pharmaceutical ingredient (API) in detail. Different forms of 122111-03-9 DMFs exist exist since differing nations have different regulations, such as 122111-03-9 USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A 122111-03-9 DMF submitted to regulatory agencies in the US is known as a USDMF. 122111-03-9 USDMF includes data on 122111-03-9's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The 122111-03-9 USDMF is kept confidential to protect the manufacturer’s intellectual property.
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We have 23 companies offering 122111-03-9
Get in contact with the supplier of your choice:
