Cohance Lifesciences, offers full range of CDMO services for small molecule APIs, intermediates, ADCs, Pellets and Formulations.
01 1M/s Cohance Lifesciences Limited
02 1M/s Apitoria Pharma Limited
03 1M/s Cipla Ltd
04 1M/s Divs Laboratories Limited
05 1M/s Nosch Labs Pvt Ltd
06 1M/s Sun Pharmaceutical Industries Limited
07 1M/s Sun Pharmaceuticals Industries ltd
08 1M/s Suven Life Sciences Limited
09 1M/s Swati Spentose Private Limited
10 1M/s Unichem Laboratories Limited
11 1M/s Vasudha Pharma Chem Limited
12 1M/s Zentiva Private Limited
13 2M/sZydus Lifesciences Limited
14 1nM/s Tyche Industries Limited
Cohance Lifesciences, offers full range of CDMO services for small molecule APIs, intermediates, ADCs, Pellets and Formulations.
Tamsulosin Hydrochloride IP/USP/Ph. Eur
Date of Issue : 2022-07-07
Valid Till : 2025-07-21
Written Confirmation Number : WC-0150
Address of the Firm : APIUnit-l,R.SNo50/1,Mukteswarapuram Village, Jaggaiahpet Mandal, NTRDistrict-521...
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PharmaCompass offers a list of Tamsulosin 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 Tamsulosin manufacturer or Tamsulosin supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Tamsulosin manufacturer or Tamsulosin supplier.
PharmaCompass also assists you with knowing the Tamsulosin API Price utilized in the formulation of products. Tamsulosin API Price is not always fixed or binding as the Tamsulosin Price is obtained through a variety of data sources. The Tamsulosin Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Pradif manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Pradif, including repackagers and relabelers. The FDA regulates Pradif manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Pradif 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 Pradif manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Pradif supplier is an individual or a company that provides Pradif active pharmaceutical ingredient (API) or Pradif finished formulations upon request. The Pradif suppliers may include Pradif API manufacturers, exporters, distributors and traders.
click here to find a list of Pradif suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Pradif written confirmation (Pradif WC) is an official document issued by a regulatory agency to a Pradif manufacturer, verifying that the manufacturing facility of a Pradif active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Pradif APIs or Pradif finished pharmaceutical products to another nation, regulatory agencies frequently require a Pradif WC (written confirmation) as part of the regulatory process.
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