DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
01 1Dr. Reddy's Laboratories Ltd.
02 1Inke S.A.
03 1F. I. S. Fabrica Italiana Sintetici S. p. A.
04 1Hetero Labs Limited
05 1LUPIN LIMITED.
06 1OLON ACTIVE PHARMACEUTICAL INGREDIENTS INDIA PRIVATE LIMITED
07 1S. A. Ajinomoto Omnichem N. V.
08 1Sanyo Chemical Research Institute Co., Ltd.
09 1Sumitomo Chemical Co., Ltd.
10 1Synthimed Labs Private Limited
11 1Zhejiang Hisoar Chuannan Pharmaceutical Co. , Ltd.
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
Registration Number : 306MF10157
Registrant's Address : 8-2-337, Road No. 3,Banjara Hills,Hyderabad 500 034,TELANGANA,INDIA
Initial Date of Registration : 2024-12-11
Latest Date of Registration : 2024-12-11
Inke S.A: APIs manufacturing plant.
Registration Number : 223MF10034
Registrant's Address : Area Industrial del Llobregat, C/Argent 1,08755 Castellbisbal Barcelona SPAIN
Initial Date of Registration : 2011-03-09
Latest Date of Registration : 2011-03-09
A Quetiapine Fumarate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Quetiapine Fumarate, including repackagers and relabelers. The FDA regulates Quetiapine Fumarate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Quetiapine Fumarate 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 Quetiapine Fumarate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Quetiapine Fumarate supplier is an individual or a company that provides Quetiapine Fumarate active pharmaceutical ingredient (API) or Quetiapine Fumarate finished formulations upon request. The Quetiapine Fumarate suppliers may include Quetiapine Fumarate API manufacturers, exporters, distributors and traders.
click here to find a list of Quetiapine Fumarate 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 Quetiapine Fumarate Drug Master File in Japan (Quetiapine Fumarate JDMF) empowers Quetiapine Fumarate 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 Quetiapine Fumarate JDMF during the approval evaluation for pharmaceutical products. At the time of Quetiapine Fumarate 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 Quetiapine Fumarate suppliers with JDMF on PharmaCompass.
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