# Zolpidem Tartrate

NDC: 0781-5317
Generic name: Zolpidem Tartrate
Labeler / Manufacturer: Sandoz Inc
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, COATED
Routes: ORAL
Marketing started: 20070423

FDA application: ANDA077322

## Active ingredients

- ZOLPIDEM TARTRATE: 5 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0781-5317"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0781-5317
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=0553e26c-f2aa-43aa-adf9-6eb951a501d3