Moehs Group, a reference company in the production of pharmaceutical active ingredients.
01 1Moehs Cantabra SL
01 1Acebutolol Hydrochloride
01 1Spain
Moehs Group, a reference company in the production of pharmaceutical active ingredients.
NDC Package Code : 68069-0009
Start Marketing Date : 2009-10-28
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
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A ACECOR HYDROCHLORIDE manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of ACECOR HYDROCHLORIDE, including repackagers and relabelers. The FDA regulates ACECOR HYDROCHLORIDE manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. ACECOR 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 ACECOR HYDROCHLORIDE manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A ACECOR HYDROCHLORIDE supplier is an individual or a company that provides ACECOR HYDROCHLORIDE active pharmaceutical ingredient (API) or ACECOR HYDROCHLORIDE finished formulations upon request. The ACECOR HYDROCHLORIDE suppliers may include ACECOR HYDROCHLORIDE API manufacturers, exporters, distributors and traders.
click here to find a list of ACECOR HYDROCHLORIDE suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA 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 ACECOR HYDROCHLORIDE as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for ACECOR 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 ACECOR 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 ACECOR HYDROCHLORIDE and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a ACECOR HYDROCHLORIDE NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of ACECOR HYDROCHLORIDE suppliers with NDC on PharmaCompass.
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