01 1MSN Laboratories Private Limited
01 1Fosnetupitant Chloride Hydrochloride
01 1India
FOSNETUPITANT CHLORIDE HYDROCHLORIDE
NDC Package Code : 14501-0105
Start Marketing Date : 2015-02-28
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
A Fosnetupitant chloride hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Fosnetupitant chloride hydrochloride, including repackagers and relabelers. The FDA regulates Fosnetupitant chloride hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Fosnetupitant chloride hydrochloride API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
A Fosnetupitant chloride hydrochloride supplier is an individual or a company that provides Fosnetupitant chloride hydrochloride active pharmaceutical ingredient (API) or Fosnetupitant chloride hydrochloride finished formulations upon request. The Fosnetupitant chloride hydrochloride suppliers may include Fosnetupitant chloride hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Fosnetupitant chloride hydrochloride suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
National Drug Code is a comprehensive database maintained by the FDA that contains information on all drugs marketed in the US. This directory includes information about finished drug products, unfinished drug products, and compounded drug products, including those containing Fosnetupitant chloride hydrochloride as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Fosnetupitant chloride hydrochloride API and other APIs are published in this directory by the FDA.
The NDC unfinished drugs database includes product listing information submitted for all unfinished drugs, such as active pharmaceutical ingredients (APIs), drugs intended for further processing and bulk drug substances for compounding.
Pharmaceutical companies that manufacture Fosnetupitant chloride hydrochloride as an active pharmaceutical ingredient (API) must furnish the FDA with an updated record of all drugs that they produce, prepare, propagate, compound, or process for commercial distribution in the US at their facilities.
The NDC directory also contains data on finished compounded human drug products that contain Fosnetupitant chloride hydrochloride and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Fosnetupitant chloride hydrochloride NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Fosnetupitant chloride hydrochloride suppliers with NDC on PharmaCompass.
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