Alchem offers Phytochemical APIs for Pharmaceuticals, Cosmetics and Nutraceuticals// FDA-inspected and EU-GMP certified.
01 1Alchem International Private Ltd
01 1Enoxolone
01 1India
Alchem offers Phytochemical APIs for Pharmaceuticals, Cosmetics and Nutraceuticals// FDA-inspected and EU-GMP certified.
NDC Package Code : 55742-130
Start Marketing Date : 2024-11-07
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
A Enoxolone manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Enoxolone, including repackagers and relabelers. The FDA regulates Enoxolone manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Enoxolone 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 Enoxolone manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Enoxolone supplier is an individual or a company that provides Enoxolone active pharmaceutical ingredient (API) or Enoxolone finished formulations upon request. The Enoxolone suppliers may include Enoxolone API manufacturers, exporters, distributors and traders.
click here to find a list of Enoxolone 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 Enoxolone as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Enoxolone 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 Enoxolone 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 Enoxolone and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Enoxolone NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Enoxolone suppliers with NDC on PharmaCompass.
We have 1 companies offering Enoxolone
Get in contact with the supplier of your choice:
LOOKING FOR A SUPPLIER?
