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Ibuprofen

NDC 71921-181, Ibuprofen, tablet, film coated, from Florida Pharmaceutical Products, LLC.

Product NDC
71921-181
Status
Listed
Labeler
Florida Pharmaceutical Products, LLC
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA071268
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/71921-181 \
  -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
71921-181-0171921018101100 TABLET, FILM COATED in 1 BOTTLE (71921-181-01)
71921-181-5071921018150500 TABLET, FILM COATED in 1 BOTTLE (71921-181-50)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/c1733fdb-5eed-2094-e053-2995a90a6c8e

Use it

Look up 71921-181 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/71921-181 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 71921-181. 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.