# IBUPROFEN, DIPHENHYDRAMINE HCL

NDC: 11673-225
Generic name: IBUPROFEN, DIPHENHYDRAMINE HCL
Labeler / Manufacturer: TARGET Corporation
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE, LIQUID FILLED
Routes: ORAL
Marketing started: 20191030

FDA application: ANDA090397

## Active ingredients

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

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"11673-225"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=11673-225
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=97e2c008-1711-dcba-e053-2995a90aa2ff