# Ibuprofen

NDC: 70512-794
Generic name: ibuprofen
Labeler / Manufacturer: SOLA Pharmaceuticals, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20250214

FDA application: ANDA202413

## Active ingredients

- IBUPROFEN: 300 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"70512-794"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70512-794
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=44fb0842-c34e-477e-96df-350cd5d6800e