Polpharma is a Polish CDMO of APIs and a significant European API producer, delivering products to companies worldwide.
01 1Pharmaceutical Works POLPHARMA S. A.
02 1Aurobindo Pharma Limited
03 1Cambrex Profarmaco Milano S. r. l.
04 1Ipca Laboratories Limited
05 1TAPI Croatia Industries Ltd.
06 1UNICHEM LABORATORIES LIMITED.
01 1HYDROCHLOROTHIAZIDE
02 3Hydrochlorothiazide
03 1Hydrochlorothiazide "Teva / Pliva"
04 1Japanese Pharmacopoeia hydrochlorothiazide
01 1Croatia
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
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
A METHYLDOPA AND HYDROCHLOROTHIAZIDE manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of METHYLDOPA AND HYDROCHLOROTHIAZIDE, including repackagers and relabelers. The FDA regulates METHYLDOPA AND HYDROCHLOROTHIAZIDE manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. METHYLDOPA AND 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 METHYLDOPA AND HYDROCHLOROTHIAZIDE manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A METHYLDOPA AND HYDROCHLOROTHIAZIDE supplier is an individual or a company that provides METHYLDOPA AND HYDROCHLOROTHIAZIDE active pharmaceutical ingredient (API) or METHYLDOPA AND HYDROCHLOROTHIAZIDE finished formulations upon request. The METHYLDOPA AND HYDROCHLOROTHIAZIDE suppliers may include METHYLDOPA AND HYDROCHLOROTHIAZIDE API manufacturers, exporters, distributors and traders.
click here to find a list of METHYLDOPA AND HYDROCHLOROTHIAZIDE 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 METHYLDOPA AND HYDROCHLOROTHIAZIDE Drug Master File in Japan (METHYLDOPA AND HYDROCHLOROTHIAZIDE JDMF) empowers METHYLDOPA AND HYDROCHLOROTHIAZIDE 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 METHYLDOPA AND HYDROCHLOROTHIAZIDE JDMF during the approval evaluation for pharmaceutical products. At the time of METHYLDOPA AND HYDROCHLOROTHIAZIDE 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 METHYLDOPA AND HYDROCHLOROTHIAZIDE suppliers with JDMF on PharmaCompass.
We have 6 companies offering METHYLDOPA AND HYDROCHLOROTHIAZIDE
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