# Ibuprofen

NDC: 11822-0231
Generic name: Ibuprofen
Labeler / Manufacturer: Rite Aid Corporation
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE, LIQUID FILLED
Routes: ORAL
Marketing started: 20200730
Marketing ended: 20261230
FDA application: ANDA078682

## Active ingredients

- IBUPROFEN: 200 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"11822-0231"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=11822-0231
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=9372c47d-2a3c-4f44-86f8-7568657844e7