Harika Drugs has been providing a qualitative range of Bulk Drugs/ APIs since 1993.
01 1M/s Harika Drugs Private Limited
02 1M/s IPCA Laboratories Ltd
01 1Promethazine HCl Ph. Eur
02 1Promethazine Hydrochloride BP/Ph.Eur./USP
01 1WC-0091n
02 1WC-0179n
01 2India
Harika Drugs has been providing a qualitative range of Bulk Drugs/ APIs since 1993.
Date of Issue : 2022-07-27
Valid Till : 2025-07-29
Written Confirmation Number : WC-0179n
Address of the Firm : Sy. No. 165/A & 165/E, Gummadidala Village, Sangareddy District, Telangana State...
Promethazine Hydrochloride BP/Ph.Eur./USP
Date of Issue : 2022-06-08
Valid Till : 2025-07-02
Written Confirmation Number : WC-0091n
Address of the Firm : P.O. Sejavta, Dist. Ratlam, Madhya Pradesh, India.
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PharmaCompass offers a list of Promethazine 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 Promethazine Hydrochloride manufacturer or Promethazine Hydrochloride supplier for your needs.
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A Histantil manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Histantil, including repackagers and relabelers. The FDA regulates Histantil manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Histantil API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A Histantil supplier is an individual or a company that provides Histantil active pharmaceutical ingredient (API) or Histantil finished formulations upon request. The Histantil suppliers may include Histantil API manufacturers, exporters, distributors and traders.
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A Histantil written confirmation (Histantil WC) is an official document issued by a regulatory agency to a Histantil manufacturer, verifying that the manufacturing facility of a Histantil active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Histantil APIs or Histantil finished pharmaceutical products to another nation, regulatory agencies frequently require a Histantil WC (written confirmation) as part of the regulatory process.
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