01 1Olon S.p.A.
01 1Oxprenolol Hydrochloride
01 1Italy
NDC Package Code : 17337-0535
Start Marketing Date : 2021-05-14
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 Oxprenolol 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 Oxprenolol manufacturer or Oxprenolol supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Oxprenolol manufacturer or Oxprenolol supplier.
PharmaCompass also assists you with knowing the Oxprenolol API Price utilized in the formulation of products. Oxprenolol API Price is not always fixed or binding as the Oxprenolol Price is obtained through a variety of data sources. The Oxprenolol Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Oxprenolol manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Oxprenolol, including repackagers and relabelers. The FDA regulates Oxprenolol manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Oxprenolol 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 Oxprenolol supplier is an individual or a company that provides Oxprenolol active pharmaceutical ingredient (API) or Oxprenolol finished formulations upon request. The Oxprenolol suppliers may include Oxprenolol API manufacturers, exporters, distributors and traders.
click here to find a list of Oxprenolol 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 Oxprenolol as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Oxprenolol 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 Oxprenolol 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 Oxprenolol and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Oxprenolol NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Oxprenolol suppliers with NDC on PharmaCompass.
