# ZOLPIDEM TARTRATE

NDC: 72722-103
Generic name: zolpidem tartrate
Labeler / Manufacturer: The ACME Laboratories Ltd.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20200924

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:"72722-103"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=72722-103
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=5679ed64-8424-4e63-a3c9-91d80fff2ca6