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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
Request
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 NDCNDC-11Package
75987-060-08759870060081 BOTTLE in 1 CARTON (75987-060-08) / 250 TABLET in 1 BOTTLE

Linked data

RxNorm, label and prices

RxNorm concepts

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
curl https://api.healthcare.dev/v1/drugs/ndc/75987-060 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
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.