01 1Arevipharma GmbH
01 1Doxapram hydrochloride monohydrate
01 1Germany
NDC Package Code : 10920-601
Start Marketing Date : 2017-10-25
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
A Doxapram Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Doxapram Hydrochloride, including repackagers and relabelers. The FDA regulates Doxapram Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Doxapram 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.
click here to find a list of Doxapram Hydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Doxapram Hydrochloride supplier is an individual or a company that provides Doxapram Hydrochloride active pharmaceutical ingredient (API) or Doxapram Hydrochloride finished formulations upon request. The Doxapram Hydrochloride suppliers may include Doxapram Hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Doxapram 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 Doxapram Hydrochloride as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Doxapram 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 Doxapram 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 Doxapram Hydrochloride and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Doxapram Hydrochloride NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Doxapram Hydrochloride suppliers with NDC on PharmaCompass.
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