# CHILDRENS IBUPROFEN

NDC: 68001-521
Generic name: Ibuprofen
Labeler / Manufacturer: BluePoint Laboratories
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SUSPENSION
Routes: ORAL
Marketing started: 20220912

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:"68001-521"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68001-521
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=d71acfe2-4643-f50b-e053-2a95a90add8b