DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
01 3Dr. Reddy's Laboratories Ltd.
02 1Teva API India Private Limited
03 1Apitoria Pharma Private Limited
04 3Aurobindo Pharma Limited
05 2DIVI'S LABORATORIES LIMITED
06 1Daito Co., Ltd.
07 3Hetero Labs Limited
08 1JUBILANT PHARMOVA LIMITED
09 1Kyowa Pharma Chemical Co., Ltd.
10 1LUPIN LIMITED.
11 1Ningbo Menovo Pharmaceutical Co. , Ltd.
12 1Shin Poong Pharm. Co. , Ltd.
13 3Sumitomo Chemical Co., Ltd.
14 1Tianish Laboratories Private Limited
15 3Zhejiang Tianyu Pharmaceutical Co. , Ltd.
16 1Zhuhai Rundu Pharmaceutical Co. , Ltd.
17 1Zydus Cadila Healthcare Ltd.
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
Registration Number : 225MF10033
Registrant's Address : 8-2-337, Road No. 3, Banjara Hills, Hyderabad 500 034, TELANGANA, INDIA
Initial Date of Registration : 2013-02-20
Latest Date of Registration : 2023-09-20
TAPI offers customized CDMO Solutions for API development and manufacturing services.
Registration Number : 225MF10043
Registrant's Address : Plot No. 2G, 2H, 2I, Udyog Vihar, Greater Noida-201 308 (U.P.) India
Initial Date of Registration : 2013-03-05
Latest Date of Registration : 2013-03-05
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
Registration Number : 305MF10042
Registrant's Address : 8-2-337, Road No. 3, Banjara Hills, Hyderabad 500 034, TELANGANA, INDIA
Initial Date of Registration : 2023-04-05
Latest Date of Registration : 2023-04-05
A Valsartan manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Valsartan, including repackagers and relabelers. The FDA regulates Valsartan manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Valsartan 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 Valsartan manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Valsartan supplier is an individual or a company that provides Valsartan active pharmaceutical ingredient (API) or Valsartan finished formulations upon request. The Valsartan suppliers may include Valsartan API manufacturers, exporters, distributors and traders.
click here to find a list of Valsartan 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 Valsartan Drug Master File in Japan (Valsartan JDMF) empowers Valsartan 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 Valsartan JDMF during the approval evaluation for pharmaceutical products. At the time of Valsartan 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 Valsartan suppliers with JDMF on PharmaCompass.
We have 16 companies offering Valsartan
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