01 1M/s. Mehta API Pvt. Ltd.,
01 1Droperidol BP/EP/USP
01 1WC-0214
01 1India
Date of Issue : 2020-02-14
Valid Till : 2022-07-02
Written Confirmation Number : WC-0214
Address of the Firm : Gut No. 546, 571, 519 & 520, Village: Kumbhavali, Tarapur, Boisar, Tal & DIst- P...
A Droperidol manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Droperidol, including repackagers and relabelers. The FDA regulates Droperidol manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Droperidol 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 Droperidol manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Droperidol supplier is an individual or a company that provides Droperidol active pharmaceutical ingredient (API) or Droperidol finished formulations upon request. The Droperidol suppliers may include Droperidol API manufacturers, exporters, distributors and traders.
click here to find a list of Droperidol suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Droperidol written confirmation (Droperidol WC) is an official document issued by a regulatory agency to a Droperidol manufacturer, verifying that the manufacturing facility of a Droperidol active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Droperidol APIs or Droperidol finished pharmaceutical products to another nation, regulatory agencies frequently require a Droperidol WC (written confirmation) as part of the regulatory process.
click here to find a list of Droperidol suppliers with Written Confirmation (WC) on PharmaCompass.
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