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 Ltd
03 1M/s. IPCA Laboratories Ltd.,
01 1Promethazine HCl (Ph. Eur.)
02 1Promethazine HCl USP
03 1Promethazine Hydrochloride (BP/USP/ Ph.Eur)
01 1WC-0091
02 1WC-0179
03 1WC-0226
01 3India
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-0179
Address of the Firm : Sy.No.165/A & 165/E, Gummadidala Village, Medak Dist,Talangana State, India
Date of Issue : 2019-10-07
Valid Till : 2022-07-02
Written Confirmation Number : WC-0226
Address of the Firm : D-24 and D24/1 MIDC Kurkumbh Tal. Daund, Dist Pune 413 802, Maharashtra State
Promethazine Hydrochloride (BP/USP/ Ph.Eur)
Date of Issue : 2022-06-08
Valid Till : 2025-07-02
Written Confirmation Number : WC-0091
Address of the Firm : Sejavta, Ratlam, Madhya Pradesh
32
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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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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