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 1Tokuyama Corporation
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
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PharmaCompass offers a list of Pioglitazone Hydrochloride 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 Pioglitazone Hydrochloride manufacturer or Pioglitazone Hydrochloride supplier for your needs.
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PharmaCompass also assists you with knowing the Pioglitazone Hydrochloride API Price utilized in the formulation of products. Pioglitazone Hydrochloride API Price is not always fixed or binding as the Pioglitazone Hydrochloride Price is obtained through a variety of data sources. The Pioglitazone Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Tox21_300584 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Tox21_300584, including repackagers and relabelers. The FDA regulates Tox21_300584 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Tox21_300584 API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A Tox21_300584 supplier is an individual or a company that provides Tox21_300584 active pharmaceutical ingredient (API) or Tox21_300584 finished formulations upon request. The Tox21_300584 suppliers may include Tox21_300584 API manufacturers, exporters, distributors and traders.
click here to find a list of Tox21_300584 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 Tox21_300584 Drug Master File in Japan (Tox21_300584 JDMF) empowers Tox21_300584 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 Tox21_300584 JDMF during the approval evaluation for pharmaceutical products. At the time of Tox21_300584 JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
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