# Ibuprofen

NDC: 71921-182
Generic name: Ibuprofen
Labeler / Manufacturer: Florida Pharmaceutical Products, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20211021

FDA application: ANDA071268

## 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:"71921-182"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=71921-182
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=c1733fdb-5eed-2094-e053-2995a90a6c8e