# glyburide

NDC: 68382-657
Generic name: glyburide
Labeler / Manufacturer: Zydus Pharmaceuticals (USA) Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20160602

FDA application: ANDA206749

## Active ingredients

- GLYBURIDE: 2.5 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"68382-657"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68382-657
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=87781ea8-62ec-483c-a4dd-8c965ce59485