# Ibuprofen Famotidine

NDC: 72189-667
Generic name: Ibuprofen Famotidine
Labeler / Manufacturer: Direct_Rx
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20260622

FDA application: ANDA218684

## Active ingredients

- IBUPROFEN: 800 mg/1
- FAMOTIDINE: 26.6 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"72189-667"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=72189-667
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=54d9e1fc-507d-1859-e063-6394a90a8c6b