01 1Wisdom Pharmaceutical Co.,Ltd
01 1Fasudil Hydrochloride Hydrate
01 1China
FASUDIL HYDROCHLORIDE HEMIHYDRATE
NDC Package Code : 13612-0025
Start Marketing Date : 2024-01-25
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
A Fasudil hydrochloride hemihydrate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Fasudil hydrochloride hemihydrate, including repackagers and relabelers. The FDA regulates Fasudil hydrochloride hemihydrate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Fasudil hydrochloride hemihydrate 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 Fasudil hydrochloride hemihydrate supplier is an individual or a company that provides Fasudil hydrochloride hemihydrate active pharmaceutical ingredient (API) or Fasudil hydrochloride hemihydrate finished formulations upon request. The Fasudil hydrochloride hemihydrate suppliers may include Fasudil hydrochloride hemihydrate API manufacturers, exporters, distributors and traders.
click here to find a list of Fasudil hydrochloride hemihydrate 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 Fasudil hydrochloride hemihydrate as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Fasudil hydrochloride hemihydrate 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 Fasudil hydrochloride hemihydrate 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 Fasudil hydrochloride hemihydrate and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Fasudil hydrochloride hemihydrate NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Fasudil hydrochloride hemihydrate suppliers with NDC on PharmaCompass.
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