# Ibuprofen

NDC: 70512-780
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: 20241201

FDA application: ANDA078329

## Active ingredients

- IBUPROFEN: 800 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"70512-780"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70512-780
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=b19b8c34-e0c1-4982-92fc-34dbe7384935