DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
01 1Dr. Reddy's Laboratories Ltd.
02 1Apitoria Pharma Private Limited
03 1Aurobindo Pharma Limited
04 1Hetero Labs Limited
05 1Hubei Gedian Humanwell Pharmaceutical Co. , Ltd.
06 1Ryoto Fine Co., Ltd.
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
Registration Number : 226MF10054
Registrant's Address : 8-2-337, Road No. 3, Banjara Hills, Hyderabad 500 034, TELANGANA, INDIA
Initial Date of Registration : 2014-03-06
Latest Date of Registration : 2021-09-02
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PharmaCompass offers a list of Finasteride 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 Finasteride manufacturer or Finasteride supplier for your needs.
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A Merck Sharp & Dohme Brand 1 of Finasteride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Merck Sharp & Dohme Brand 1 of Finasteride, including repackagers and relabelers. The FDA regulates Merck Sharp & Dohme Brand 1 of Finasteride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Merck Sharp & Dohme Brand 1 of Finasteride 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 Merck Sharp & Dohme Brand 1 of Finasteride supplier is an individual or a company that provides Merck Sharp & Dohme Brand 1 of Finasteride active pharmaceutical ingredient (API) or Merck Sharp & Dohme Brand 1 of Finasteride finished formulations upon request. The Merck Sharp & Dohme Brand 1 of Finasteride suppliers may include Merck Sharp & Dohme Brand 1 of Finasteride API manufacturers, exporters, distributors and traders.
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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 Merck Sharp & Dohme Brand 1 of Finasteride Drug Master File in Japan (Merck Sharp & Dohme Brand 1 of Finasteride JDMF) empowers Merck Sharp & Dohme Brand 1 of Finasteride 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 Merck Sharp & Dohme Brand 1 of Finasteride JDMF during the approval evaluation for pharmaceutical products. At the time of Merck Sharp & Dohme Brand 1 of Finasteride 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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We have 5 companies offering Merck Sharp & Dohme Brand 1 of Finasteride
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