# IBUPROFEN PM

NDC: 21130-623
Generic name: diphenhydramine citrate, ibuprofen
Labeler / Manufacturer: Safeway
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20251229

FDA application: ANDA079113

## Active ingredients

- DIPHENHYDRAMINE CITRATE: 38 mg/1
- IBUPROFEN: 200 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"21130-623"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=21130-623
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=57e8f0d7-1f21-4fda-8b21-3caa54fae4e6