Nuray is an expert in the synthesis of Niche novel APIs, the first to launch Generics, NCEs, Advanced Intermediates // USFDA certified.
01 1NURAY CHEMICALS PRIVATE LIMITED
02 1CU Chemie Uetikon GmbH
03 1PCAS
04 1DARMERICA, LLC
05 1MEDISCA INC.
06 1Medisca Inc.
07 1Patheon Inc.
08 1SHODHANA LABORATORIES PRIVATE LIMITED
09 1SPICA LABORATORIES PRIVATE LIMITED
10 1SYNFINE DRUGS PRIVATE LIMITED
11 1Sri Krishna Pharmaceuticals Ltd. Unit I
01 1SODIUM PHENYLBUTERATE
02 2SODIUM PHENYLBUTYRATE
03 1Sodium Phenyl butyrate
04 5Sodium Phenylbutyrate
05 1Sodium Phenylbutyrate (SPB)
06 1sodium phenylbutyrate and ursodoxicoltaurine
01 2France
02 3India
03 4U.S.A
04 2Blank
Nuray is an expert in the synthesis of Niche novel APIs, the first to launch Generics, NCEs, Advanced Intermediates // USFDA certified.
NDC Package Code : 58159-095
Start Marketing Date : 2023-04-13
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (35kg/35kg)
Marketing Category : BULK INGREDIENT
Seqens is an integrated global leader in pharmaceutical solutions & specialty ingredients & provides custom-made solutions.
NDC Package Code : 54382-120
Start Marketing Date : 1997-06-10
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Seqens is an integrated global leader in pharmaceutical solutions & specialty ingredients & provides custom-made solutions.
NDC Package Code : 68925-0010
Start Marketing Date : 2024-01-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 71052-297
Start Marketing Date : 2021-01-29
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 38779-2549
Start Marketing Date : 2014-07-08
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 38779-3207
Start Marketing Date : 2020-02-05
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
SODIUM PHENYLBUTYRATE; TAURURSODIOL
NDC Package Code : 66406-0338
Start Marketing Date : 2022-09-29
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (3g/14600g 1g/14600g)
Marketing Category : DRUG FOR FURTHER PROCESSING
NDC Package Code : 69056-006
Start Marketing Date : 2024-08-20
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 66326-504
Start Marketing Date : 2011-06-06
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 83875-002
Start Marketing Date : 2024-03-20
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (500kg/500kg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
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A Sodium Phenylbutyrate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Sodium Phenylbutyrate, including repackagers and relabelers. The FDA regulates Sodium Phenylbutyrate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Sodium 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 Sodium Phenylbutyrate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Sodium Phenylbutyrate supplier is an individual or a company that provides Sodium Phenylbutyrate active pharmaceutical ingredient (API) or Sodium Phenylbutyrate finished formulations upon request. The Sodium Phenylbutyrate suppliers may include Sodium Phenylbutyrate API manufacturers, exporters, distributors and traders.
click here to find a list of Sodium 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 Sodium Phenylbutyrate as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Sodium 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 Sodium 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 Sodium Phenylbutyrate and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Sodium Phenylbutyrate NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Sodium Phenylbutyrate suppliers with NDC on PharmaCompass.
We have 7 companies offering Sodium Phenylbutyrate
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