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IBUPROFEN

NDC 72189-231, IBUPROFEN, tablet, film coated, from DIRECT RX.

Product NDC
72189-231
Status
Listed
Labeler
DIRECT RX
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA090796
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/72189-231 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • IBUPROFEN600 mg/1

Pharmacologic classes

Anti-Inflammatory Agents, Non-Steroidal [CS]; Cyclooxygenase Inhibitors [MoA]; Nonsteroidal Anti-inflammatory Drug [EPC]

Package NDCNDC-11Package
72189-231-217218902312121 TABLET, FILM COATED in 1 BOTTLE (72189-231-21)
72189-231-307218902313030 TABLET, FILM COATED in 1 BOTTLE (72189-231-30)
72189-231-607218902316060 TABLET, FILM COATED in 1 BOTTLE (72189-231-60)
72189-231-907218902319090 TABLET, FILM COATED in 1 BOTTLE (72189-231-90)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/c3f30813-0848-6e8a-e053-2995a90a3dea

Use it

Look up 72189-231 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/72189-231 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 72189-231. 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.