01 1AX Pharmaceutical Corp
02 1Pharma Source Direct, Inc.
03 1Professional Compounding Centers of America
04 2Seratec S.A.S.
01 1QUINACRINE HYDROCHLORIDE
02 1Quinacrine
03 1Quinacrine Dihydrochloride
04 1Quinacrine Dihydrochloride Dihydrate
05 1Quinacrine dihydrochloride dihydrate
01 1Canada
02 2France
03 1U.S.A
04 1United Kingdom
NDC Package Code : 73377-034
Start Marketing Date : 2020-03-18
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 51927-0322
Start Marketing Date : 2023-10-16
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 82393-307
Start Marketing Date : 2023-10-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 65732-201
Start Marketing Date : 2023-07-25
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 65732-202
Start Marketing Date : 2023-07-25
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
A Quinacrine Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Quinacrine Hydrochloride, including repackagers and relabelers. The FDA regulates Quinacrine Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Quinacrine 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 Quinacrine Hydrochloride supplier is an individual or a company that provides Quinacrine Hydrochloride active pharmaceutical ingredient (API) or Quinacrine Hydrochloride finished formulations upon request. The Quinacrine Hydrochloride suppliers may include Quinacrine Hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Quinacrine 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 Quinacrine Hydrochloride as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Quinacrine 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 Quinacrine 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 Quinacrine Hydrochloride and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Quinacrine Hydrochloride NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Quinacrine Hydrochloride suppliers with NDC on PharmaCompass.
We have 4 companies offering Quinacrine Hydrochloride
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