76325-496 : Buphenyl 500 mg/1 Oral Tablet


NDC76325-496
Labeler: Hyperion Therapeutics, Inc.
Product Type: Human Prescription Drug
Drug Name:  Buphenyl
Dosage Form: Oral Tablet
Application #: NDA020572
Rev. Date: 


Appearance:


Shapes:  Oval
Colors:  White
Size (mm): 16
Segments: * 1

* Segments = the number of equally sized pieces which the pill can be broken into. In this case, a value of 1 indicates a solid pill with no score lines.

NDC Package Codes:

  • 76325-496-03: 1 BOTTLE IN 1 CARTON (76325‑496‑03) > 250 TABLET IN 1 BOTTLE

Active Ingredients:

  • Sodium Phenylbutyrate

Dosage Strength:

  • 500 mg

Inactive Ingredients:

  • Cellulose, Microcrystalline
  • Silicon Dioxide
  • Magnesium Stearate

Pharmaceutical Classes:

  • Ammonium Ion Binding Activity [MoA]
  • Nitrogen Binding Agent [EPC]

Related Products:

Based on records with the same trade name.
  • 76325-188 Buphenyl .94 g/g Oral Powder by Hyperion Therapeutics, Inc.
  • 62592-188 Buphenyl .94 g/g Oral Powder by Ucyclyd Pharma Inc.
  • 62592-496 Buphenyl 500 mg Oral Tablet by Ucyclyd Pharma Inc.
  • 75987-060 Buphenyl 500 mg Oral Tablet by Horizon Pharma, Inc.
  • 75987-070 Buphenyl .94 g/g Oral Powder by Horizon Pharma, Inc.

NDC QR Code

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Note: The RxChat NDC Database uses publicly available data from the FDA and the U.S. National Library of Medicine (NLM); The NLM is not responsible for the data presented and does not endorse or recommend this or any other product. While we make every effort to ensure that the information presented is accurate, you should assume that all results are unvalidated. To report any errors or inconsistencies please contact us.