# Ibuprofen

NDC: 53746-137
Generic name: Ibuprofen
Labeler / Manufacturer: Amneal Pharmaceuticals of New York LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20090105

FDA application: ANDA071935

## Active ingredients

- IBUPROFEN: 800 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"53746-137"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=53746-137
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=75d963b9-3675-44ff-bc6b-83461bed1b67