TAPI offers customized CDMO Solutions for API development and manufacturing services.
01 1Teva API India Private Limited
02 1Hetero Drugs Limited
03 1Patheon Austria GmbH & CoKG
01 1Glycerol Phenyl Butyrate
02 1Glycerol phenylbutyrate
03 1glycerol phenylbutyrate
01 1India
02 1Israel
03 1U.S.A
TAPI offers customized CDMO Solutions for API development and manufacturing services.
NDC Package Code : 15894-0037
Start Marketing Date : 2021-01-27
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 65977-0121
Start Marketing Date : 2013-02-01
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 45941-3054
Start Marketing Date : 2012-01-10
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
A Glycerol Phenylbutyrate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Glycerol Phenylbutyrate, including repackagers and relabelers. The FDA regulates Glycerol Phenylbutyrate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Glycerol Phenylbutyrate 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 Glycerol Phenylbutyrate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Glycerol Phenylbutyrate supplier is an individual or a company that provides Glycerol Phenylbutyrate active pharmaceutical ingredient (API) or Glycerol Phenylbutyrate finished formulations upon request. The Glycerol Phenylbutyrate suppliers may include Glycerol Phenylbutyrate API manufacturers, exporters, distributors and traders.
click here to find a list of Glycerol Phenylbutyrate 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 Glycerol Phenylbutyrate as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Glycerol Phenylbutyrate 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 Glycerol Phenylbutyrate 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 Glycerol Phenylbutyrate and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Glycerol Phenylbutyrate NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Glycerol Phenylbutyrate suppliers with NDC on PharmaCompass.
We have 3 companies offering Glycerol Phenylbutyrate
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