01 1M/s Sun Pharmaceuticals Industries ltd
02 1M/sMSN Life Sciences Pvt Ltd
01 1Tiagabine Hydrochloride IH/USP
02 1Tiagabine Hydrochloride USP
01 1WC-0168
02 1WC-0383
01 2India
Date of Issue : 2022-08-08
Valid Till : 2025-08-08
Written Confirmation Number : WC-0383
Address of the Firm : Unit-ll, Sy No * Parts of 454,455,457,458 & 459 Chandampet-Village, Shankarampet...
Tiagabine Hydrochloride IH/USP
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 Tiagabine Hydrochloride 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 Tiagabine Hydrochloride manufacturer or Tiagabine Hydrochloride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Tiagabine Hydrochloride manufacturer or Tiagabine Hydrochloride supplier.
PharmaCompass also assists you with knowing the Tiagabine Hydrochloride API Price utilized in the formulation of products. Tiagabine Hydrochloride API Price is not always fixed or binding as the Tiagabine Hydrochloride Price is obtained through a variety of data sources. The Tiagabine Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A CEP-6671 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of CEP-6671, including repackagers and relabelers. The FDA regulates CEP-6671 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. CEP-6671 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 CEP-6671 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A CEP-6671 supplier is an individual or a company that provides CEP-6671 active pharmaceutical ingredient (API) or CEP-6671 finished formulations upon request. The CEP-6671 suppliers may include CEP-6671 API manufacturers, exporters, distributors and traders.
click here to find a list of CEP-6671 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A CEP-6671 written confirmation (CEP-6671 WC) is an official document issued by a regulatory agency to a CEP-6671 manufacturer, verifying that the manufacturing facility of a CEP-6671 active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting CEP-6671 APIs or CEP-6671 finished pharmaceutical products to another nation, regulatory agencies frequently require a CEP-6671 WC (written confirmation) as part of the regulatory process.
click here to find a list of CEP-6671 suppliers with Written Confirmation (WC) on PharmaCompass.
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