# IBUPROFEN

NDC: 62207-320
Generic name: IBUPROFEN
Labeler / Manufacturer: Granules India Limited
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20191114

FDA application: ANDA202312

## 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:"62207-320"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=62207-320
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=97516b9f-219a-429d-850d-1fe9fd66646b