# Ibuprofen PM

NDC: 30142-278
Generic name: Ibuprofen and Diphenhydramine Citrate
Labeler / Manufacturer: KROGER COMPANY
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, COATED
Routes: ORAL
Marketing started: 20240507

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:"30142-278"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=30142-278
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=15e649c4-d75f-e8c1-e063-6294a90a7747