# pain relief pm

NDC: 69452-264
Generic name: IBUPROFEN, 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: 20190501

FDA application: ANDA090397

## Active ingredients

- DIPHENHYDRAMINE HYDROCHLORIDE: 25 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:"69452-264"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=69452-264
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=58666a5c-fc92-4c8d-9c04-f0c98dc05c56