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 1Archimica
05 1Benzo Chem Industries Pvt
06 1Cipla
07 1Dishman Carbogen Amcis
08 2Emcure Pharmaceuticals
09 1Fresenius Kabi AB Brunna
10 1GLAND CHEMICALS PRIVATE LIMITED
11 2Hansoh Pharma
12 1Hetero Drugs
13 2Intas Pharmaceuticals
14 1JARI Pharmaceutical
15 1Laurus Labs
16 1MSN Laboratories
17 1Olon S.p.A
18 1PharmaEssentia
19 1ScinoPharm Taiwan, Ltd
20 2Shilpa Medicare
21 1Sun Pharmaceutical Industries Limited
22 1Viatris
23 1Yangtze River Pharmaceutical Group
24 1Zhejiang Hisun Pharmaceutical
25 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 offers customized CDMO Solutions for API development and manufacturing services.
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 offers customized CDMO Solutions for API development and manufacturing services.
GDUFA
DMF Review : Complete
Rev. Date : 2015-02-20
Pay. Date : 2013-08-20
DMF Number : 27402
Submission : 2014-02-20
Status :
Type : II
A Gemcitabine Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Gemcitabine Hydrochloride, including repackagers and relabelers. The FDA regulates Gemcitabine Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Gemcitabine Hydrochloride API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
click here to find a list of Gemcitabine Hydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Gemcitabine Hydrochloride supplier is an individual or a company that provides Gemcitabine Hydrochloride active pharmaceutical ingredient (API) or Gemcitabine Hydrochloride finished formulations upon request. The Gemcitabine Hydrochloride suppliers may include Gemcitabine Hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Gemcitabine Hydrochloride suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Gemcitabine Hydrochloride DMF (Drug Master File) is a document detailing the whole manufacturing process of Gemcitabine Hydrochloride active pharmaceutical ingredient (API) in detail. Different forms of Gemcitabine Hydrochloride DMFs exist exist since differing nations have different regulations, such as Gemcitabine Hydrochloride USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Gemcitabine Hydrochloride DMF submitted to regulatory agencies in the US is known as a USDMF. Gemcitabine Hydrochloride USDMF includes data on Gemcitabine Hydrochloride's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Gemcitabine Hydrochloride USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Gemcitabine Hydrochloride suppliers with USDMF on PharmaCompass.
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