# Ibuprofen and Diphenhydramine Citrate

NDC: 58602-867
Generic name: Ibuprofen and Diphenhydramine Citrate
Labeler / Manufacturer: Aurohealth LLC
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, COATED
Routes: ORAL
Marketing started: 20220531

FDA application: ANDA216204

## 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:"58602-867"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=58602-867
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=21c1f5c5-19fa-4a59-bad3-ea85fd37471b