# Etodolac

NDC: 51672-4036
Generic name: Etodolac
Labeler / Manufacturer: Taro Pharmaceuticals U.S.A., Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20000425

FDA application: ANDA075074

## Active ingredients

- ETODOLAC: 500 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"51672-4036"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=51672-4036
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=ec82b108-6a6f-4d1b-82cb-831d4ed36c80