01 1Kalchem International inc
02 2Sigma-Aldrich Ireland Ltd.
01 1ACEPROMAZINE MALEATE
02 2Acepromazine Maleate
01 3U.S.A
NDC Package Code : 60592-430
Start Marketing Date : 2020-01-03
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 54154-028
Start Marketing Date : 2024-10-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (25kg/25kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 54154-019
Start Marketing Date : 2010-03-29
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (25kg/25kg)
Marketing Category : BULK INGREDIENT
A Acepromazine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Acepromazine, including repackagers and relabelers. The FDA regulates Acepromazine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Acepromazine 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 Acepromazine supplier is an individual or a company that provides Acepromazine active pharmaceutical ingredient (API) or Acepromazine finished formulations upon request. The Acepromazine suppliers may include Acepromazine API manufacturers, exporters, distributors and traders.
click here to find a list of Acepromazine 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 Acepromazine as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Acepromazine 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 Acepromazine 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 Acepromazine and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Acepromazine NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Acepromazine suppliers with NDC on PharmaCompass.
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