# pain relief pm

NDC: 69452-507
Generic name: IBUPROFEN AND DIPHENHYDRAMINE HCL
Labeler / Manufacturer: Bionpharma Inc.
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE, LIQUID FILLED
Routes: ORAL
Marketing started: 20260520

FDA application: ANDA090397

## Active ingredients

- IBUPROFEN: 200 mg/1
- DIPHENHYDRAMINE HYDROCHLORIDE: 25 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"69452-507"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=69452-507
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=51037299-37dd-ca57-e063-6394a90a12c7