Evonik's CDMO solutions for APIs and HPAPIs: It specializes where the client needs it most!
01 1Evonik Rexim S.A.S
02 10818396d-cc18-00ac-e063-6394a90a5d82
03 2Ajinomoto Health & Nutrition North America Inc.
04 1Shanghai Kyowa Amino Acid Co., Ltd
01 3L-PROLINE
02 1L-Proline
03 1Proline
01 1Germany
02 3Japan
03 1Blank
Evonik's CDMO solutions for APIs and HPAPIs: It specializes where the client needs it most!
NDC Package Code : 51593-5012
Start Marketing Date : 1992-09-03
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 51495-828
Start Marketing Date : 2022-10-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 51495-028
Start Marketing Date : 2022-10-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 74920-009
Start Marketing Date : 2020-03-09
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (20kg/20kg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 51927-5235
Start Marketing Date : 2023-10-19
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
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PharmaCompass offers a list of Proline 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 Proline manufacturer or Proline supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Proline manufacturer or Proline supplier.
PharmaCompass also assists you with knowing the Proline API Price utilized in the formulation of products. Proline API Price is not always fixed or binding as the Proline Price is obtained through a variety of data sources. The Proline Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A PRO (IUPAC abbreviation) manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of PRO (IUPAC abbreviation), including repackagers and relabelers. The FDA regulates PRO (IUPAC abbreviation) manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. PRO (IUPAC abbreviation) 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 PRO (IUPAC abbreviation) manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A PRO (IUPAC abbreviation) supplier is an individual or a company that provides PRO (IUPAC abbreviation) active pharmaceutical ingredient (API) or PRO (IUPAC abbreviation) finished formulations upon request. The PRO (IUPAC abbreviation) suppliers may include PRO (IUPAC abbreviation) API manufacturers, exporters, distributors and traders.
click here to find a list of PRO (IUPAC abbreviation) 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 PRO (IUPAC abbreviation) as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for PRO (IUPAC abbreviation) 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 PRO (IUPAC abbreviation) 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 PRO (IUPAC abbreviation) and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a PRO (IUPAC abbreviation) NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of PRO (IUPAC abbreviation) suppliers with NDC on PharmaCompass.
We have 3 companies offering PRO (IUPAC abbreviation)
Get in contact with the supplier of your choice:
