01 2M/s Azico Biophore India
02 1M/s Azico Biophore India Pvt Ltd
03 1M/s. Sun Pharmaceuticals Ltd.
01 1Liothyronin sodium EP
02 2Liothyronin sodium USP
03 1Liothyronine Sodium USP
01 1WC-0168
02 1WC-0404
03 1WC-0404A2
04 1WC-0404A3
01 4India
Date of Issue : 2021-02-26
Valid Till : 2023-06-22
Written Confirmation Number : WC-0404A3
Address of the Firm : Plot No.40/A Sy.13,15,16,51,52 &182 J.N Pharma City Thanam village Parawada mand...
Date of Issue : 2020-08-17
Valid Till : 2023-06-22
Written Confirmation Number : WC-0404
Address of the Firm : Plot No.40/A Sy.13,15,16,51,52 &182 J.N Pharma City Thanam village Parawada mand...
Date of Issue : 2020-08-17
Valid Till : 2023-06-22
Written Confirmation Number : WC-0404A2
Address of the Firm : Plot No.40/A Sy.13,15,16,51,52 &182 J.N Pharma City Thanam village Parawada mand...
Date of Issue : 2022-08-08
Valid Till : 2025-07-14
Written Confirmation Number : WC-0168
Address of the Firm : Plot No. 24/2, & 25, Phase -IV, GIDC, Industrial Zone, At & Post - Panoli, Dist....
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PharmaCompass offers a list of Liothyronine Sodium 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 Liothyronine Sodium manufacturer or Liothyronine Sodium supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Liothyronine Sodium manufacturer or Liothyronine Sodium supplier.
PharmaCompass also assists you with knowing the Liothyronine Sodium API Price utilized in the formulation of products. Liothyronine Sodium API Price is not always fixed or binding as the Liothyronine Sodium Price is obtained through a variety of data sources. The Liothyronine Sodium Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Triostat manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Triostat, including repackagers and relabelers. The FDA regulates Triostat manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Triostat 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 Triostat manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Triostat supplier is an individual or a company that provides Triostat active pharmaceutical ingredient (API) or Triostat finished formulations upon request. The Triostat suppliers may include Triostat API manufacturers, exporters, distributors and traders.
click here to find a list of Triostat suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Triostat written confirmation (Triostat WC) is an official document issued by a regulatory agency to a Triostat manufacturer, verifying that the manufacturing facility of a Triostat active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Triostat APIs or Triostat finished pharmaceutical products to another nation, regulatory agencies frequently require a Triostat WC (written confirmation) as part of the regulatory process.
click here to find a list of Triostat suppliers with Written Confirmation (WC) on PharmaCompass.
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