01 1Curia Italy S.r.l.
02 1DARMERICA, LLC
03 1Piramal Pharma Limited
01 1MECAMYLAMINE HYDROCHLORIDE
02 1MGF (Mechano Growth Factor) Acetate
03 1Mecamylamine Hydrochloride
01 3U.S.A
NDC Package Code : 55486-1563
Start Marketing Date : 2012-06-03
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (25kg/25kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 71052-828
Start Marketing Date : 2021-03-30
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 65085-0075
Start Marketing Date : 2022-08-03
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
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PharmaCompass offers a list of Mecamylamine Hydrochloride API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Mecamylamine Hydrochloride manufacturer or Mecamylamine Hydrochloride supplier for your needs.
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PharmaCompass also assists you with knowing the Mecamylamine Hydrochloride API Price utilized in the formulation of products. Mecamylamine Hydrochloride API Price is not always fixed or binding as the Mecamylamine Hydrochloride Price is obtained through a variety of data sources. The Mecamylamine Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A MECASERMIN RECOMBINANT manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of MECASERMIN RECOMBINANT, including repackagers and relabelers. The FDA regulates MECASERMIN RECOMBINANT manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. MECASERMIN RECOMBINANT 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 MECASERMIN RECOMBINANT supplier is an individual or a company that provides MECASERMIN RECOMBINANT active pharmaceutical ingredient (API) or MECASERMIN RECOMBINANT finished formulations upon request. The MECASERMIN RECOMBINANT suppliers may include MECASERMIN RECOMBINANT API manufacturers, exporters, distributors and traders.
click here to find a list of MECASERMIN RECOMBINANT 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 MECASERMIN RECOMBINANT as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for MECASERMIN RECOMBINANT 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 MECASERMIN RECOMBINANT 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 MECASERMIN RECOMBINANT and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a MECASERMIN RECOMBINANT NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of MECASERMIN RECOMBINANT suppliers with NDC on PharmaCompass.
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