01 1Chattem Chemicals, Inc.
02 1Embio Limited
01 2Hydroxyamphetamine Hydrobromide
01 1India
02 1U.S.A
HYDROXYAMPHETAMINE HYDROBROMIDE
NDC Package Code : 61960-6300
Start Marketing Date : 1999-03-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
HYDROXYAMPHETAMINE HYDROBROMIDE
NDC Package Code : 60646-105
Start Marketing Date : 2011-03-30
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
A HYDROXYAMPHETAMINE HYDROBROMIDE manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of HYDROXYAMPHETAMINE HYDROBROMIDE, including repackagers and relabelers. The FDA regulates HYDROXYAMPHETAMINE HYDROBROMIDE manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. HYDROXYAMPHETAMINE HYDROBROMIDE 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 HYDROXYAMPHETAMINE HYDROBROMIDE supplier is an individual or a company that provides HYDROXYAMPHETAMINE HYDROBROMIDE active pharmaceutical ingredient (API) or HYDROXYAMPHETAMINE HYDROBROMIDE finished formulations upon request. The HYDROXYAMPHETAMINE HYDROBROMIDE suppliers may include HYDROXYAMPHETAMINE HYDROBROMIDE API manufacturers, exporters, distributors and traders.
click here to find a list of HYDROXYAMPHETAMINE HYDROBROMIDE 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 HYDROXYAMPHETAMINE HYDROBROMIDE as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for HYDROXYAMPHETAMINE HYDROBROMIDE 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 HYDROXYAMPHETAMINE HYDROBROMIDE 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 HYDROXYAMPHETAMINE HYDROBROMIDE and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a HYDROXYAMPHETAMINE HYDROBROMIDE NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of HYDROXYAMPHETAMINE HYDROBROMIDE suppliers with NDC on PharmaCompass.
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