# Ibuprofen

NDC: 57344-109
Generic name: Ibuprofen
Labeler / Manufacturer: AAA Pharmaceutical, Inc.
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, COATED
Routes: ORAL
Marketing started: 20121001

FDA application: ANDA079129

## Active ingredients

- IBUPROFEN: 200 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"57344-109"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=57344-109
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=fbc7fb61-d295-464b-9f3b-52262ed6f31a