# IBUPROFEN

NDC: 59556-895
Generic name: IBUPROFEN
Labeler / Manufacturer: Strides Pharma Inc
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE, LIQUID FILLED
Routes: ORAL
Marketing started: 20221116

FDA application: ANDA204469

## Active ingredients

- IBUPROFEN: 200 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"59556-895"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=59556-895
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=69b208ff-83f5-40d1-a2ff-d54b390e46e4