# IBUPROFEN AND FAMOTIDINE

NDC: 85509-1315
Generic name: Ibuprofen and famotidine
Labeler / Manufacturer: PHOENIX RX LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20230315

FDA application: ANDA216814

## Active ingredients

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

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"85509-1315"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=85509-1315
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=3ff33400-30e8-87fa-e063-6394a90a7f5c