01 1Curia Italy s.r.l.
02 1Olon Ricerca Bioscience, LLC
03 1Olon SpA
01 2Aceclidine HCl
02 1Aceclidine Hydrochloride
01 2Italy
02 1U.S.A
NDC Package Code : 55486-1608
Start Marketing Date : 2024-09-19
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 71604-0002
Start Marketing Date : 2022-10-24
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 17337-0058
Start Marketing Date : 2014-08-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
A Aceclidine Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Aceclidine Hydrochloride, including repackagers and relabelers. The FDA regulates Aceclidine Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Aceclidine 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 Aceclidine Hydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Aceclidine Hydrochloride supplier is an individual or a company that provides Aceclidine Hydrochloride active pharmaceutical ingredient (API) or Aceclidine Hydrochloride finished formulations upon request. The Aceclidine Hydrochloride suppliers may include Aceclidine Hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Aceclidine 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 Aceclidine Hydrochloride as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Aceclidine 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 Aceclidine 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 Aceclidine Hydrochloride and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Aceclidine Hydrochloride NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Aceclidine Hydrochloride suppliers with NDC on PharmaCompass.
We have 2 companies offering Aceclidine Hydrochloride
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