# Ibuprofen

NDC: 21130-745
Generic name: Ibuprofen
Labeler / Manufacturer: Safeway, Inc.
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE, LIQUID FILLED
Routes: ORAL
Marketing started: 20180228
Marketing ended: 20270228
FDA application: ANDA206568

## 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:"21130-745"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=21130-745
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=a530d43d-e9c4-4edb-af66-c92860e46f45