# Ibuprofen and Diphenhydramine Citrate

NDC: 55111-565
Generic name: Ibuprofen and Diphenhydramine Citrate
Labeler / Manufacturer: Dr. Reddy's Laboratories Limited
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20100131

FDA application: ANDA090619

## 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:"55111-565"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=55111-565
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=42c06daf-541a-7721-b875-ea18364501a4