Biophore is a research-driven global pharmaceutical company focused on niche APIs for the generic industry.
01 1Biophore India Pharmaceuticals Pvt. Ltd
02 1DOTTIKON EXCLUSIVE SYNTHESIS AG
03 2Dipharma Francis S.r.l.
04 1Honour Lab Limited
05 1Maithri Drugs Private Limited
06 1Seven Star Pharmaceutical Co., Ltd.
07 1Solara Active Pharma Sciences Limited
08 1Teva Pharmaceutical Works Private Limited Company
01 6Sapropterin Dihydrochloride
02 2Sapropterin dihydrochloride
03 1Sapropterine Dihydrochloride
01 4India
02 1Israel
03 2Italy
04 1Switzerland
05 1Taiwan
Biophore is a research-driven global pharmaceutical company focused on niche APIs for the generic industry.
NDC Package Code : 73435-017
Start Marketing Date : 2021-12-06
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (10kg/10kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 46438-0660
Start Marketing Date : 2020-12-11
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 46438-0664
Start Marketing Date : 2021-12-17
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 54864-872
Start Marketing Date : 2007-12-14
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 69037-0048
Start Marketing Date : 2013-12-19
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 70600-062
Start Marketing Date : 2024-11-14
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 66652-2103
Start Marketing Date : 2019-01-21
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 72643-026
Start Marketing Date : 2021-09-21
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 51846-1057
Start Marketing Date : 2019-08-16
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (100kg/100kg)
Marketing Category : BULK INGREDIENT
A Sapropterin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Sapropterin, including repackagers and relabelers. The FDA regulates Sapropterin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Sapropterin 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 Sapropterin manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Sapropterin supplier is an individual or a company that provides Sapropterin active pharmaceutical ingredient (API) or Sapropterin finished formulations upon request. The Sapropterin suppliers may include Sapropterin API manufacturers, exporters, distributors and traders.
click here to find a list of Sapropterin 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 Sapropterin as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Sapropterin 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 Sapropterin 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 Sapropterin and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Sapropterin NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Sapropterin suppliers with NDC on PharmaCompass.
We have 8 companies offering Sapropterin
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