# Zolpidem tartrate sublingual

NDC: 49884-899
Generic name: Zolpidem tartrate sublingual
Labeler / Manufacturer: Par Health USA, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: SUBLINGUAL
Marketing started: 20170911

FDA application: ANDA204229

## Active ingredients

- ZOLPIDEM TARTRATE: 3.5 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"49884-899"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=49884-899
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=44b34e58-114b-4774-9fab-4b188dfe0228