# Ibuprofen and Diphenhydramine Citrate

NDC: 21130-228
Generic name: Ibuprofen and Diphenhydramine Citrate
Labeler / Manufacturer: Better Living Brands, LLC
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, COATED
Routes: ORAL
Marketing started: 20231115

FDA application: ANDA216204

## Active ingredients

- DIPHENHYDRAMINE CITRATE: 38 mg/1
- IBUPROFEN: 200 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"21130-228"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=21130-228
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=fcfb044d-f6b9-5c43-e053-6394a90ac417