# Ibuprofen

NDC: 11822-0894
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: 20200131
Marketing ended: 20261231
FDA application: ANDA206999

## Active ingredients

- IBUPROFEN: 200 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"11822-0894"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=11822-0894
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=47657d95-4a54-49c2-8273-86b413b8f41e