Seqens is an integrated global leader in pharmaceutical solutions & specialty ingredients, & custom-made solutions to our customers.
01 1PCAS FRANCE
02 1Siegfried Evionnaz SA
01 1OXYBUTYNIN BASE
02 1Oxybutynin
01 1France
02 1Switzerland
Seqens is an integrated global leader in pharmaceutical solutions & specialty ingredients, & custom-made solutions to our customers.
NDC Package Code : 49169-1013
Start Marketing Date : 2009-08-14
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 17381-015
Start Marketing Date : 2010-04-20
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
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PharmaCompass offers a list of Oxybutynin 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 Oxybutynin manufacturer or Oxybutynin supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Oxybutynin manufacturer or Oxybutynin supplier.
PharmaCompass also assists you with knowing the Oxybutynin API Price utilized in the formulation of products. Oxybutynin API Price is not always fixed or binding as the Oxybutynin Price is obtained through a variety of data sources. The Oxybutynin Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Cystonorm manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Cystonorm, including repackagers and relabelers. The FDA regulates Cystonorm manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Cystonorm 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 Cystonorm manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Cystonorm supplier is an individual or a company that provides Cystonorm active pharmaceutical ingredient (API) or Cystonorm finished formulations upon request. The Cystonorm suppliers may include Cystonorm API manufacturers, exporters, distributors and traders.
click here to find a list of Cystonorm 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 Cystonorm as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Cystonorm 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 Cystonorm 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 Cystonorm and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Cystonorm NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Cystonorm suppliers with NDC on PharmaCompass.
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