# IBUPROFEN CA

NDC: 11673-990
Generic name: IBUPROFEN
Labeler / Manufacturer: TARGET CORPORATION
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, COATED
Routes: ORAL
Marketing started: 20200101

FDA application: ANDA091239

## Active ingredients

- IBUPROFEN: 200 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"11673-990"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=11673-990
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=8e8684fa-095e-c6d6-e053-2a95a90a15b4