Polpharma is a Polish CDMO of APIs and a significant European API producer, delivering products to companies worldwide.
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01 1Pharmaceutical Works POLPHARMA S. A.
02 1Aurobindo Pharma Limited
03 1Cambrex Profarmaco Milano S. r. l.
04 1Ipca Laboratories Limited
05 2TAPI Croatia Industries Ltd.
06 1UNICHEM LABORATORIES LIMITED.
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01 1HYDROCHLOROTHIAZIDE
02 4Hydrochlorothiazide
03 1Hydrochlorothiazide "Teva / Pliva"
04 1Japanese Pharmacopoeia hydrochlorothiazide
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01 2Croatia
02 3India
03 1Poland
04 1U.S.A
Polpharma is a Polish CDMO of APIs and a significant European API producer, delivering products to companies worldwide.
Registration Number : 218MF11020
Registrant's Address : 19 Pellinska Str. 83-200 Starogard Gdanski POLAND
Initial Date of Registration : 2006-12-28
Latest Date of Registration : 2024-07-11
Registration Number : 224MF10214
Registrant's Address : Plot No. 2, Maitrivihar, Ameerpet, Hyderabad Andhra Pradesh, India
Initial Date of Registration : 2012-11-08
Latest Date of Registration : 2012-11-08
Registration Number : 219MF10334
Registrant's Address : Via Curiel 34, 20067 Paulo, Milano, ITALY
Initial Date of Registration : 2007-11-20
Latest Date of Registration : 2018-10-01
Registration Number : 224MF10171
Registrant's Address : 48, Kandivli Industrial Estate, Kandivli (W), Mumbai 400 067, India
Initial Date of Registration : 2012-08-16
Latest Date of Registration : 2021-09-02
Registration Number : 307MF10004
Registrant's Address : Prudnicka cesta 54, Savski Marof, County Brdovec 10291 Prigorje Brdovecko, Croatia
Initial Date of Registration : 2025-01-09
Latest Date of Registration : 2025-01-09
Hydrochlorothiazide "Teva/Pliva"
Registration Number : 229MF10218
Registrant's Address : Prudnicka cesta 54, Savski Marof, County Brdovec 10291 Prigorje Brdovecko, Croatia
Initial Date of Registration : 2017-12-12
Latest Date of Registration : 2017-12-12
Japanese Pharmacopoeia Hydrochlorothiazide
Registration Number : 225MF10021
Registrant's Address : Unichem Bhavan, Prabhat Estate, S. V. Road, Jogeshwari (West), Mumbai-400 102, India
Initial Date of Registration : 2013-02-06
Latest Date of Registration : 2013-02-06
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PharmaCompass offers a list of Hydrochlorothiazide 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 Hydrochlorothiazide manufacturer or Hydrochlorothiazide supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Hydrochlorothiazide manufacturer or Hydrochlorothiazide supplier.
PharmaCompass also assists you with knowing the Hydrochlorothiazide API Price utilized in the formulation of products. Hydrochlorothiazide API Price is not always fixed or binding as the Hydrochlorothiazide Price is obtained through a variety of data sources. The Hydrochlorothiazide Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Esidrex manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Esidrex, including repackagers and relabelers. The FDA regulates Esidrex manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Esidrex 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 Esidrex manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Esidrex supplier is an individual or a company that provides Esidrex active pharmaceutical ingredient (API) or Esidrex finished formulations upon request. The Esidrex suppliers may include Esidrex API manufacturers, exporters, distributors and traders.
click here to find a list of Esidrex suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
The Pharmaceuticals and Medical Devices Agency (PMDA) established the Japan Drug Master File (JDMF), also known as the Master File (MF), to permit Japanese and foreign manufacturers of drug substances, intermediates, excipients, raw materials, and packaging materials (‘Products’) to voluntarily register confidential information about the production and management of their products in Japan.
The Esidrex Drug Master File in Japan (Esidrex JDMF) empowers Esidrex API manufacturers to present comprehensive information (e.g., production methods, data, etc.) to the review authority, i.e., PMDA (Pharmaceuticals & Medical Devices Agency).
PMDA reviews the Esidrex JDMF during the approval evaluation for pharmaceutical products. At the time of Esidrex JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
click here to find a list of Esidrex suppliers with JDMF on PharmaCompass.
We have 6 companies offering Esidrex
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