# CHILDRENS IBUPROFEN

NDC: 21130-216
Generic name: IBUPROFEN
Labeler / Manufacturer: Better Living Brands, LLC
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SUSPENSION
Routes: ORAL
Marketing started: 20250321

FDA application: ANDA209179

## Active ingredients

- IBUPROFEN: 100 mg/5mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"21130-216"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=21130-216
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=fab39a0a-882b-bf96-e053-6294a90a2932