# IBUPROFEN

NDC: 11673-993
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: ANDA091237

## 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:"11673-993"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=11673-993
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=8e872c8d-28e2-cd49-e053-2995a90a469f