75987-060 : Buphenyl 500 mg Oral Tablet
NDC: | 75987-060 |
Labeler: | Horizon Pharma, Inc. |
Product Type: | Human Prescription Drug |
Drug Name: | Buphenyl |
Dosage Form: | Oral Tablet |
Application #: | NDA020573 |
Rev. Date: |
Appearance:
Markings: | UCY;500 |
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:
- 75987-060-08: 1 BOTTLE IN 1 CARTON (75987‑060‑08) > 250 TABLET IN 1 BOTTLE
Active Ingredients:
- Sodium Phenylbutyrate
Dosage Strength:
- 500 mg
Pharmaceutical Classes:
- Ammonium Ion Binding Activity [MoA]
- Nitrogen Binding Agent [EPC]
Related Products:
Based on records with the same trade name.- 75987-070 Buphenyl .94 g/g Oral Powder by Horizon Pharma, Inc.
- 62592-188 Buphenyl .94 g/g Oral Powder by Ucyclyd Pharma Inc.
- 62592-496 Buphenyl 500 mg Oral Tablet by Ucyclyd Pharma Inc.
- 76325-188 Buphenyl .94 g/g Oral Powder by Hyperion Therapeutics, Inc.
- 76325-496 Buphenyl 500 mg/1 Oral Tablet by Hyperion Therapeutics, 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.