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01 1M/s. Centauar Pharmacerticals Pvt. Ltd.,
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01 1Brotizolam (EP)
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01 1WC-0107
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01 1India
Date of Issue : 2022-06-08
Valid Till : 2025-06-25
Written Confirmation Number : WC-0107
Address of the Firm : Plot No. 75/76, Chikhloli, MIDC, Ambernath (W), Dist- Thane 421501 Maharashtra ...
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PharmaCompass offers a list of Brotizolam 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 Brotizolam manufacturer or Brotizolam supplier for your needs.
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PharmaCompass also assists you with knowing the Brotizolam API Price utilized in the formulation of products. Brotizolam API Price is not always fixed or binding as the Brotizolam Price is obtained through a variety of data sources. The Brotizolam Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Lendormin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Lendormin, including repackagers and relabelers. The FDA regulates Lendormin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Lendormin 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 Lendormin manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Lendormin supplier is an individual or a company that provides Lendormin active pharmaceutical ingredient (API) or Lendormin finished formulations upon request. The Lendormin suppliers may include Lendormin API manufacturers, exporters, distributors and traders.
click here to find a list of Lendormin suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Lendormin written confirmation (Lendormin WC) is an official document issued by a regulatory agency to a Lendormin manufacturer, verifying that the manufacturing facility of a Lendormin active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Lendormin APIs or Lendormin finished pharmaceutical products to another nation, regulatory agencies frequently require a Lendormin WC (written confirmation) as part of the regulatory process.
click here to find a list of Lendormin suppliers with Written Confirmation (WC) on PharmaCompass.
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