# Ibuprofen

NDC: 68998-011
Generic name: Ibuprofen
Labeler / Manufacturer: Marc Glassman, Inc.
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, COATED
Routes: ORAL
Marketing started: 20200501

FDA application: ANDA202312

## Active ingredients

- IBUPROFEN: 200 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"68998-011"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68998-011
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=9714e804-fadb-103d-e053-2a95a90ad765