# GLYBURIDE

NDC: 23155-058
Generic name: GLYBURIDE
Labeler / Manufacturer: Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20101005

FDA application: ANDA090937

## Active ingredients

- GLYBURIDE: 5 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"23155-058"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=23155-058
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=33418bba-c5ea-4c0f-9d28-31dc2724c6c3