Harika Drugs has been providing a qualitative range of Bulk Drugs/ APIs since 1993.
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01 1M/s Harika Drugs Private Limited
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01 1Promethazine HCl Ph. Eur
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01 1WC-0179n
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01 1India
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...
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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.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Promethazine Hydrochloride manufacturer or Promethazine Hydrochloride supplier.
PharmaCompass also assists you with knowing the Promethazine Hydrochloride API Price utilized in the formulation of products. Promethazine Hydrochloride API Price is not always fixed or binding as the Promethazine Hydrochloride Price is obtained through a variety of data sources. The Promethazine Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Allerfen manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Allerfen, including repackagers and relabelers. The FDA regulates Allerfen manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Allerfen 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 Allerfen supplier is an individual or a company that provides Allerfen active pharmaceutical ingredient (API) or Allerfen finished formulations upon request. The Allerfen suppliers may include Allerfen API manufacturers, exporters, distributors and traders.
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A Allerfen written confirmation (Allerfen WC) is an official document issued by a regulatory agency to a Allerfen manufacturer, verifying that the manufacturing facility of a Allerfen active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Allerfen APIs or Allerfen finished pharmaceutical products to another nation, regulatory agencies frequently require a Allerfen WC (written confirmation) as part of the regulatory process.
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