Harika Drugs has been providing a qualitative range of Bulk Drugs/ APIs since 1993.
01 1M/s Harika Drugs Private Limited
02 1M/s Emcure Pharmaceuticals Limited
01 1Promethazine HCl EP
02 1Promethazine Hydrochloride EP
01 1WC-0179n
02 1WC-0226
01 2India
Harika Drugs has been providing a qualitative range of Bulk Drugs/ APIs since 1993.
Date of Issue : 2025-10-15
Valid Till : 2028-07-29
Written Confirmation Number : WC-0179n
Address of the Firm : Sy. No. 165/A & 165/E, Gummadidala Village, Gummadidala (Mandal), Dist.- Sangare...
Date of Issue : 2025-09-26
Valid Till : 2028-07-02
Written Confirmation Number : WC-0226
Address of the Firm : D-24 & D-24/1, M.I.D.C., Kurkumbh, Taluka: Daund, District. Pune -413802, Mahara...
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A HL 8700 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of HL 8700, including repackagers and relabelers. The FDA regulates HL 8700 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. HL 8700 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 HL 8700 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A HL 8700 supplier is an individual or a company that provides HL 8700 active pharmaceutical ingredient (API) or HL 8700 finished formulations upon request. The HL 8700 suppliers may include HL 8700 API manufacturers, exporters, distributors and traders.
click here to find a list of HL 8700 suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PharmaCompass.
A HL 8700 written confirmation (HL 8700 WC) is an official document issued by a regulatory agency to a HL 8700 manufacturer, verifying that the manufacturing facility of a HL 8700 active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting HL 8700 APIs or HL 8700 finished pharmaceutical products to another nation, regulatory agencies frequently require a HL 8700 WC (written confirmation) as part of the regulatory process.
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