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OLPRUVA

NDC 72542-667, sodium phenylbutyrate, kit, from Acer Therapeutics Inc..

Product NDC
72542-667
Status
Listed
Labeler
Acer Therapeutics Inc.
Dosage form
KIT
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
NDA
Application
NDA214860
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/72542-667 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

None listed.

Package NDCNDC-11Package
72542-667-187254206671890 BOX in 1 CARTON (72542-667-18) / 1 KIT in 1 BOX (72542-667-02) * 1 FOR SUSPENSION in 1 PACKET (72542-367-01) * 1 FOR SUSPENSION in 1 PACKET (72542-000-01) * 1 FOR SUSPENSION in 1 PACKET (72542-003-01)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/89abc31c-43e8-4809-9eb7-172cb31a86f1

Use it

Look up 72542-667 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/72542-667 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 72542-667. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.
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Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.