# Ibuprofen PM

NDC: 41250-050
Generic name: diphenhydramine citrate, ibuprofen
Labeler / Manufacturer: Meijer Distribution Inc
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20090408

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:"41250-050"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=41250-050
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=47e71e23-da8a-4759-ac5a-1d48e0d9ab98