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IBUPROFEN

NDC 72189-324, IBUPROFEN, tablet, film coated, from Direct Rx.

Product NDC
72189-324
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/72189-324 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • IBUPROFEN400 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
72189-324-307218903243030 TABLET, FILM COATED in 1 BOTTLE (72189-324-30)
72189-324-607218903246060 TABLET, FILM COATED in 1 BOTTLE (72189-324-60)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/d88d0544-57a7-4a82-e053-2a95a90a1945

Use it

Look up 72189-324 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/72189-324 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 72189-324. 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.