Polpharma is a Polish CDMO of APIs and a significant European API producer, delivering products to companies worldwide.
01 1ZAKŁADY FARMACEUTYCZNE POLPHARMA S.A. Starogard Gdański PL
02 2TEVA PHARMACEUTICAL INDUSTRIES LTD Tel Aviv - Jaffa IL
03 1ALEMBIC PHARMACEUTICALS LIMITED Vadodara IN
04 2AMOLI ORGANICS PRIVATE LIMITED Mumbai IN
05 2APITORIA PHARMA PRIVATE LIMITED Hyderabad IN
06 1AREVIPHARMA GMBH Radebeul DE
07 1BLUE CIRCLE ORGANICS PRIVATE LIMITED Ambernath West IN
08 1CTX LIFESCIENCES PVT. LIMITED Surat IN
09 1Cambrex Profarmaco Milano S.r.l. Paullo IT
10 1Changzhou Pharmaceutical Factory Jiangsu Province CN
11 1FLAMMA S.P.A. Chignolo d'Isola IT
12 3IPCA LABORATORIES LIMITED Mumbai IN
13 1MACLEODS PHARMACEUTICALS LIMITED Mumbai IN
14 1Posh Chemicals Private Limited Hyderabad IN
15 1SOUTHWEST SYNTHETIC PHARMACEUTICAL CORPORATION, LIMITED Chongqing CN
16 1SUZHOU LIXIN PHARMACEUTICAL CO., LTD. Suzhou CN
17 2Unichem Laboratories Limited Mumbai IN
18 1ZHEJIANG HUAHAI PHARMACEUTICAL CO., LTD. Linhai CN
01 16Hydrochlorothiazide
02 1Hydrochlorothiazide, Form-I
03 1Hydrochlorothiazide, Process 2
04 1Hydrochlorothiazide, Process I
05 1Hydrochlorothiazide, Process II
06 1Hydrochlorothiazide, Process III
07 1Hydrochlorothiazide, Process-II
08 1Hydrochlorothiazide, Process-II, Form-I
09 1Hydrochlorothiazide, Standard grade, micronised grade
01 4China
02 1Germany
03 14India
04 2Israel
05 1Italy
06 1Poland
07 1U.S.A
01 4Expired
02 19Valid
03 1Withdrawn by Holder
Polpharma is a Polish CDMO of APIs and a significant European API producer, delivering products to companies worldwide.
Polpharma is a Polish CDMO of APIs and a significant European API producer, delivering products to companies worldwide.
Hydrochlorothiazide, Standard Grade, Micronised ...
Certificate Number : CEP 2004-058 - Rev 06
Status : Valid
Issue Date : 2024-04-12
Type : Chemical
Substance Number : 394
TAPI, a leading global supplier of APIs, provides over 350 products and customized CDMO solutions for every stage of development.
TAPI, a leading global supplier of APIs, provides over 350 products and customized CDMO solutions for every stage of development.
Certificate Number : R1-CEP 2001-304 - Rev 12
Status : Valid
Issue Date : 2022-10-03
Type : Chemical
Substance Number : 394
TAPI, a leading global supplier of APIs, provides over 350 products and customized CDMO solutions for every stage of development.
TAPI, a leading global supplier of APIs, provides over 350 products and customized CDMO solutions for every stage of development.
Certificate Number : R1-CEP 2004-149 - Rev 07
Status : Valid
Issue Date : 2022-10-03
Type : Chemical
Substance Number : 394
Hydrochlorothiazide, Process-II, Form-I
Certificate Number : CEP 2024-362 - Rev 00
Status : Valid
Issue Date : 2024-11-18
Type : Chemical
Substance Number : 394
Certificate Number : CEP 2005-013 - Rev 06
Status : Valid
Issue Date : 2023-11-16
Type : Chemical
Substance Number : 394
Certificate Number : R1-CEP 2008-021 - Rev 05
Status : Valid
Issue Date : 2023-08-29
Type : Chemical
Substance Number : 394
Hydrochlorothiazide, Process I
Certificate Number : R1-CEP 2004-013 - Rev 06
Status : Valid
Issue Date : 2023-08-29
Type : Chemical
Substance Number : 394
Certificate Number : CEP 2021-088 - Rev 00
Status : Valid
Issue Date : 2024-01-23
Type : Chemical
Substance Number : 394
Hydrochlorothiazide, Process 2
Certificate Number : CEP 2020-017 - Rev 01
Status : Valid
Issue Date : 2024-11-12
Type : Chemical
Substance Number : 394
Certificate Number : CEP 2009-060 - Rev 02
Status : Valid
Issue Date : 2023-11-14
Type : Chemical
Substance Number : 394
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 CEP of the European Pharmacopoeia monograph is often referred to as a Hydrochlorothiazide Certificate of Suitability (COS). The purpose of a Hydrochlorothiazide CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Hydrochlorothiazide EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Hydrochlorothiazide to their clients by showing that a Hydrochlorothiazide CEP has been issued for it. The manufacturer submits a Hydrochlorothiazide CEP (COS) as part of the market authorization procedure, and it takes on the role of a Hydrochlorothiazide CEP holder for the record. Additionally, the data presented in the Hydrochlorothiazide CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Hydrochlorothiazide DMF.
A Hydrochlorothiazide CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Hydrochlorothiazide CEPs may be accepted in nations that are not members of the Ph. Eur. at the discretion of the authorities there.
click here to find a list of Hydrochlorothiazide suppliers with CEP (COS) on PharmaCompass.
We have 18 companies offering Hydrochlorothiazide
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