# ibuprofen pm

NDC: 11822-0050
Generic name: Diphenhydramine Citrate, Ibuprofen
Labeler / Manufacturer: Rite Aid Corporation
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20090319
Marketing ended: 20261031
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:"11822-0050"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=11822-0050
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=d9eefb84-cc2e-4deb-a1c0-a7c21929f5ac