# IBUPROFEN 200 MG

NDC: 0761-0908
Generic name: IBUPROFEN
Labeler / Manufacturer: Basic Drugs, Inc.
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20211214

FDA application: ANDA079174

## 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:"0761-0908"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0761-0908
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=d3351d44-2078-3adc-e053-2995a90a3c8f