01 1AmbioPharm, Inc.
02 1DARMERICA, LLC
03 1MSN Life Sciences Private Limited
04 1Olon S.p.A.
05 1Polypeptide Laboratories Inc
01 5Teduglutide
01 1India
02 1Italy
03 1Switzerland
04 2U.S.A
NDC Package Code : 41524-0009
Start Marketing Date : 2017-12-12
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 71052-036
Start Marketing Date : 2024-11-21
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 69766-106
Start Marketing Date : 2022-12-14
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 17337-0264
Start Marketing Date : 2021-10-27
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 63557-1031
Start Marketing Date : 2022-04-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (100g/100g)
Marketing Category : BULK INGREDIENT
A Teduglutide manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Teduglutide, including repackagers and relabelers. The FDA regulates Teduglutide manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Teduglutide 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 Teduglutide manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Teduglutide supplier is an individual or a company that provides Teduglutide active pharmaceutical ingredient (API) or Teduglutide finished formulations upon request. The Teduglutide suppliers may include Teduglutide API manufacturers, exporters, distributors and traders.
click here to find a list of Teduglutide 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 Teduglutide as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Teduglutide 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 Teduglutide 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 Teduglutide and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Teduglutide NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Teduglutide suppliers with NDC on PharmaCompass.
We have 5 companies offering Teduglutide
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