DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
01 2Dr. Reddy's Laboratories Ltd.
02 1Teva API India Private Limited
03 1Assia Chemical Industries Ltd.
04 1Aurobindo Pharma Limited
05 2Daito Co., Ltd.
06 1HANMI FINE CHEMICAL CO. , LTD.
07 1Hamari PFST Co., Ltd.
08 2Hetero Labs Limited
09 1Ipca Laboratories Limited
10 1JUBILANT PHARMOVA LIMITED
11 1KOLON LIFE SCIENCE, INC.
12 1Quimica Syntetica S. A.
13 1Tianish Laboratories Private Limited
14 2Zhejiang Huahai Pharmaceutical Co. , Ltd.
15 1Zydus Cadila Healthcare Ltd.
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
Registration Number : 222MF10263
Registrant's Address : 8-2-337, Road No. 3, Banjara Hills, Hyderabad 500 034, TELANGANA, INDIA
Initial Date of Registration : 2010-11-29
Latest Date of Registration : 2023-03-29
TAPI, a leading global supplier of APIs, provides over 350 products and customized CDMO solutions for every stage of development.
Losartan potassium "Teva/Malanpur"
Registration Number : 230MF10060
Registrant's Address : Plot No. 2G, 2H, 2I, Udyog Vihar, Greater Noida-201 308 (U.P.) India
Initial Date of Registration : 2018-05-08
Latest Date of Registration : 2018-05-08
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
Registration Number : 304MF10068
Registrant's Address : 8-2-337, Road No. 3, Banjara Hills, Hyderabad 500 034, TELANGANA, INDIA
Initial Date of Registration : 2022-04-20
Latest Date of Registration : 2022-04-20
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PharmaCompass offers a list of Losartan Potassium 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 Losartan Potassium manufacturer or Losartan Potassium supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Losartan Potassium manufacturer or Losartan Potassium supplier.
PharmaCompass also assists you with knowing the Losartan Potassium API Price utilized in the formulation of products. Losartan Potassium API Price is not always fixed or binding as the Losartan Potassium Price is obtained through a variety of data sources. The Losartan Potassium Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Losartan manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Losartan, including repackagers and relabelers. The FDA regulates Losartan manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Losartan 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 Losartan manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Losartan supplier is an individual or a company that provides Losartan active pharmaceutical ingredient (API) or Losartan finished formulations upon request. The Losartan suppliers may include Losartan API manufacturers, exporters, distributors and traders.
click here to find a list of Losartan 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 Losartan Drug Master File in Japan (Losartan JDMF) empowers Losartan 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 Losartan JDMF during the approval evaluation for pharmaceutical products. At the time of Losartan 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 Losartan suppliers with JDMF on PharmaCompass.
We have 15 companies offering Losartan
Get in contact with the supplier of your choice:
