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, a leading global supplier of APIs, provides over 350 products and customized CDMO solutions for every stage of development.
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
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PharmaCompass offers a list of Valsartan 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 Valsartan manufacturer or Valsartan supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Valsartan manufacturer or Valsartan supplier.
PharmaCompass also assists you with knowing the Valsartan API Price utilized in the formulation of products. Valsartan API Price is not always fixed or binding as the Valsartan Price is obtained through a variety of data sources. The Valsartan Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Diovan manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Diovan, including repackagers and relabelers. The FDA regulates Diovan manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Diovan 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 Diovan manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Diovan supplier is an individual or a company that provides Diovan active pharmaceutical ingredient (API) or Diovan finished formulations upon request. The Diovan suppliers may include Diovan API manufacturers, exporters, distributors and traders.
click here to find a list of Diovan 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 Diovan Drug Master File in Japan (Diovan JDMF) empowers Diovan 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 Diovan JDMF during the approval evaluation for pharmaceutical products. At the time of Diovan 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 Diovan suppliers with JDMF on PharmaCompass.
We have 16 companies offering Diovan
Get in contact with the supplier of your choice:
