# Zolpidem

NDC: 80425-0430
Generic name: Zolpidem Tartrate
Labeler / Manufacturer: Advanced Rx of Tennessee, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20240813

FDA application: ANDA077214

## Active ingredients

- ZOLPIDEM TARTRATE: 5 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"80425-0430"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=80425-0430
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=1fa86b79-8809-35f4-e063-6394a90a4377