# Ibuprofen

NDC: 11822-6604
Generic name: Ibuprofen
Labeler / Manufacturer: Rite Aid Corporation
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20200904
Marketing ended: 20270228
FDA application: ANDA072096

## 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:"11822-6604"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=11822-6604
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=1dba3cb7-2e3d-4378-93cf-92db8f24f41f