Cohance Lifesciences, offers full range of CDMO services for small molecule APIs, intermediates, ADCs, Pellets and Formulations.
01 1Avra Laboratories Pvt. Ltd.
01 1S-8-Ethyl-8-hydroxy-2,3,5,8-tetrahydro-6-oxa-3-aza-cyclopenta naphthalene-1,4,7-trione
01 1India
Cohance Lifesciences, offers full range of CDMO services for small molecule APIs, intermediates, ADCs, Pellets and Formulations.
4-ETHYL-4-HYDROXY-7,8-DIHYDRO-1H-PYRANO(3,4-F)INDOLIZINE-3,6,10(4H)-TRIONE, (S)-
NDC Package Code : 70772-0005
Start Marketing Date : 2024-05-01
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (25kg/25kg)
Marketing Category : BULK INGREDIENT
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PharmaCompass offers a list of N-Desethyloxybutynin API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, and more, enabling you to easily find the right N-Desethyloxybutynin manufacturer or N-Desethyloxybutynin supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred N-Desethyloxybutynin manufacturer or N-Desethyloxybutynin supplier.
A N-Desethyloxybutynin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of N-Desethyloxybutynin, including repackagers and relabelers. The FDA regulates N-Desethyloxybutynin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. N-Desethyloxybutynin 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 N-Desethyloxybutynin supplier is an individual or a company that provides N-Desethyloxybutynin active pharmaceutical ingredient (API) or N-Desethyloxybutynin finished formulations upon request. The N-Desethyloxybutynin suppliers may include N-Desethyloxybutynin API manufacturers, exporters, distributors and traders.
click here to find a list of N-Desethyloxybutynin 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 N-Desethyloxybutynin as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for N-Desethyloxybutynin 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 N-Desethyloxybutynin 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 N-Desethyloxybutynin and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a N-Desethyloxybutynin NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of N-Desethyloxybutynin suppliers with NDC on PharmaCompass.
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