Polpharma is a Polish CDMO of APIs and a significant European API producer, delivering products to companies worldwide.
01 1Polpharma
02 1Sanofi
03 2TAPI Technology & API Services
04 2Abbott Laboratories
05 1Alembic Pharmaceuticals Limited
06 1Amoli Organics
07 1AstraZeneca
08 1Aurobindo Pharma Limited
09 1CTX Lifesciences
10 1Cambrex Corporation
11 2Changzhou Pharmaceutical Factory
12 1Daiichi Sankyo
13 2GSK
14 1Industriale Chimica
15 2Ipca Laboratories
16 1Macleods Pharmaceuticals Limited
17 1Medimpex
18 1Posh Chemicals P. Ltd
19 1Suzhou Lixin Pharmaceutical
20 3Unichem Laboratories Limited
21 1Zhejiang Huahai Pharmaceutical
22 1Zydus Lifesciences
23 2Blank
Polpharma is a Polish CDMO of APIs and a significant European API producer, delivering products to companies worldwide.
GDUFA
DMF Review : Complete
Rev. Date : 2015-01-06
Pay. Date : 2014-12-29
DMF Number : 17599
Submission : 2004-08-12
Status :
Type : II
Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 5125
Submission : 1983-11-07
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 : 2012-11-30
Pay. Date : 2012-11-08
DMF Number : 2115
Submission : 1973-06-14
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 : 2012-11-30
Pay. Date : 2012-11-08
DMF Number : 4028
Submission : 1980-12-10
Status :
Type : II
A Hydrochlorothiazide manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Hydrochlorothiazide, including repackagers and relabelers. The FDA regulates Hydrochlorothiazide manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Hydrochlorothiazide 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 Hydrochlorothiazide manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Hydrochlorothiazide supplier is an individual or a company that provides Hydrochlorothiazide active pharmaceutical ingredient (API) or Hydrochlorothiazide finished formulations upon request. The Hydrochlorothiazide suppliers may include Hydrochlorothiazide API manufacturers, exporters, distributors and traders.
click here to find a list of Hydrochlorothiazide suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Hydrochlorothiazide DMF (Drug Master File) is a document detailing the whole manufacturing process of Hydrochlorothiazide active pharmaceutical ingredient (API) in detail. Different forms of Hydrochlorothiazide DMFs exist exist since differing nations have different regulations, such as Hydrochlorothiazide USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Hydrochlorothiazide DMF submitted to regulatory agencies in the US is known as a USDMF. Hydrochlorothiazide USDMF includes data on Hydrochlorothiazide's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Hydrochlorothiazide USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Hydrochlorothiazide suppliers with USDMF on PharmaCompass.
We have 22 companies offering Hydrochlorothiazide
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