# Ibuprofen PM

NDC: 69607-1970
Generic name: Diphenhydramine Citrate, Ibuprofen
Labeler / Manufacturer: WR Group, Inc.
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, COATED
Routes: ORAL
Marketing started: 20250228

FDA application: ANDA211404

## 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:"69607-1970"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=69607-1970
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=1e2feaf0-7fff-43d5-bcfe-9f2851bdc805