# Etodolac

NDC: 0093-1118
Generic name: Etodolac
Labeler / Manufacturer: Teva Pharmaceuticals USA, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20000817

FDA application: ANDA075665

## Active ingredients

- ETODOLAC: 600 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0093-1118"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0093-1118
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=f3bf1675-8fda-40d3-8427-0a6a6133a3d3