DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
01 1Dr.Reddy's Laboratories Limited
02 1B.V. KATWIJK CHEMIE
01 1OXAPROZIN
02 1Oxaprozin
01 1India
02 1Netherlands
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
NDC Package Code : 55111-013
Start Marketing Date : 1999-09-30
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 17349-0008
Start Marketing Date : 1995-01-18
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (50kg/50kg)
Marketing Category : BULK INGREDIENT
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PharmaCompass offers a list of Oxaprozin 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 Oxaprozin manufacturer or Oxaprozin supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Oxaprozin manufacturer or Oxaprozin supplier.
PharmaCompass also assists you with knowing the Oxaprozin API Price utilized in the formulation of products. Oxaprozin API Price is not always fixed or binding as the Oxaprozin Price is obtained through a variety of data sources. The Oxaprozin Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Oxaprozin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Oxaprozin, including repackagers and relabelers. The FDA regulates Oxaprozin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Oxaprozin 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 Oxaprozin manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Oxaprozin supplier is an individual or a company that provides Oxaprozin active pharmaceutical ingredient (API) or Oxaprozin finished formulations upon request. The Oxaprozin suppliers may include Oxaprozin API manufacturers, exporters, distributors and traders.
click here to find a list of Oxaprozin 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 Oxaprozin as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Oxaprozin 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 Oxaprozin 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 Oxaprozin and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Oxaprozin NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Oxaprozin suppliers with NDC on PharmaCompass.
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