# Ibuprofen and famotidine

NDC: 67877-626
Generic name: Ibuprofen and famotidine
Labeler / Manufacturer: Ascend Laboratories, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20210804

FDA application: ANDA211890

## 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:"67877-626"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=67877-626
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=4493d4cd-ca8e-4b0a-9b65-b75e55bf8b9e