# Childrens Ibuprofen Oral Suspension

NDC: 0121-0833
Generic name: Ibuprofen
Labeler / Manufacturer: PAI Holdings, LLC dba PAI Pharma
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SUSPENSION
Routes: ORAL
Marketing started: 20250801

FDA application: ANDA214789

## 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:"0121-0833"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0121-0833
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=c26cefe0-182a-4b03-baeb-b3eb2e0e2267