Nuray is an expert in the synthesis of Niche novel APIs, the first to launch Generics, NCEs, Advanced Intermediates // USFDA certified.
01 1NURAY CHEMICALS PRIVATE LIMITED
02 1Moehs Cantabra SL
01 2Acebutolol Hydrochloride
01 1India
02 1Spain
Nuray is an expert in the synthesis of Niche novel APIs, the first to launch Generics, NCEs, Advanced Intermediates // USFDA certified.
NDC Package Code : 58159-081
Start Marketing Date : 2020-10-08
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (35kg/35kg)
Marketing Category : BULK INGREDIENT
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 : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
A Acebutolol Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Acebutolol Hydrochloride, including repackagers and relabelers. The FDA regulates Acebutolol Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Acebutolol 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 Acebutolol Hydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Acebutolol Hydrochloride supplier is an individual or a company that provides Acebutolol Hydrochloride active pharmaceutical ingredient (API) or Acebutolol Hydrochloride finished formulations upon request. The Acebutolol Hydrochloride suppliers may include Acebutolol Hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Acebutolol 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 Acebutolol Hydrochloride as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Acebutolol 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 Acebutolol 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 Acebutolol Hydrochloride and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Acebutolol Hydrochloride NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Acebutolol Hydrochloride suppliers with NDC on PharmaCompass.
We have 2 companies offering Acebutolol Hydrochloride
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