BUPHENYL
NDC 75987-060, sodium phenylbutyrate, tablet, from Horizon Therapeutics USA, Inc..
- Product NDC
- 75987-060
- Status
- Listed
- Labeler
- Horizon Therapeutics USA, Inc.
- Dosage form
- TABLET
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- NDA
- Application
- NDA020572
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/75987-060 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- SODIUM PHENYLBUTYRATE500 mg/1
Pharmacologic classes
Ammonium Ion Binding Activity [MoA]; Nitrogen Binding Agent [EPC]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 75987-060-08 | 75987006008 | 1 BOTTLE in 1 CARTON (75987-060-08) / 250 TABLET in 1 BOTTLE |
Linked data
RxNorm, label and prices
Related lookups
FDA label sections
GET /v1/drugs/labels/463a36fa-3eb2-4326-8bd0-c8c7a11bca3a
Use it
Look up 75987-060 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/75987-060 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 75987-060. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.
Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.