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Ibuprofen Famotidine

NDC 72189-667, Ibuprofen Famotidine, tablet, from Direct_Rx.

Product NDC
72189-667
Status
Listed
Labeler
Direct_Rx
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA218684
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/72189-667 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • IBUPROFEN800 mg/1
  • FAMOTIDINE26.6 mg/1

Pharmacologic classes

Anti-Inflammatory Agents, Non-Steroidal [CS]; Cyclooxygenase Inhibitors [MoA]; Histamine H2 Receptor Antagonists [MoA]; Histamine-2 Receptor Antagonist [EPC]; Nonsteroidal Anti-inflammatory Drug [EPC]

Package NDCNDC-11Package
72189-667-907218906679090 TABLET in 1 BOTTLE (72189-667-90)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/54d9e1fc-507d-1859-e063-6394a90a8c6b

Use it

Look up 72189-667 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/72189-667 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 72189-667. 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.