# Ketoprofen

NDC: 0276-0507
Generic name: Ketoprofen
Labeler / Manufacturer: Misemer Pharmaceuticals, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE
Routes: ORAL
Marketing started: 20250523

FDA application: ANDA074014

## Active ingredients

- KETOPROFEN: 75 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0276-0507"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0276-0507
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=d0f47ab6-29ff-df07-e053-2a95a90a2b51