DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
01 1Dr. Reddy's Laboratories Ltd.
02 1HANMI FINE CHEMICAL CO. , LTD.
03 1HETERO DRUGS LIMITED.
04 1Hetero Labs Limited
05 1Juzen Chemical Co., Ltd.
06 1MSN Organics Private Limited.
07 1Ohara Pharmaceutical Co., Ltd.
08 1Polaris AI Pharma Corp.
09 1Sanyo Chemical Research Institute Co., Ltd.
10 1Tokuyama Corporation
11 1ZaCh System S. A.
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
Registration Number : 303MF10161
Registrant's Address : 8-2-337, Road No. 3, Banjara Hills, Hyderabad 500 034, TELANGANA, INDIA
Initial Date of Registration : 2021-10-27
Latest Date of Registration : 2021-10-27
A Pioglitazone Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Pioglitazone Hydrochloride, including repackagers and relabelers. The FDA regulates Pioglitazone Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Pioglitazone 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 Pioglitazone Hydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Pioglitazone Hydrochloride supplier is an individual or a company that provides Pioglitazone Hydrochloride active pharmaceutical ingredient (API) or Pioglitazone Hydrochloride finished formulations upon request. The Pioglitazone Hydrochloride suppliers may include Pioglitazone Hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Pioglitazone Hydrochloride 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 Pioglitazone Hydrochloride Drug Master File in Japan (Pioglitazone Hydrochloride JDMF) empowers Pioglitazone Hydrochloride 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 Pioglitazone Hydrochloride JDMF during the approval evaluation for pharmaceutical products. At the time of Pioglitazone Hydrochloride 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 Pioglitazone Hydrochloride suppliers with JDMF on PharmaCompass.
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