# Ibuprofen 200 mg and Diphenhydramine Citrate 38 mg

NDC: 63548-0197
Generic name: Ibuprofen, Diphenhydramine Citrate
Labeler / Manufacturer: PLD Acquisitions LLC DBA Avma Pharma Solutions
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20240411

FDA application: ANDA211404

## 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:"63548-0197"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=63548-0197
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=a7d729bf-6d7a-415a-a414-cae0ba6d0063