# Xanax

NDC: 0009-0090
Generic name: alprazolam
Labeler / Manufacturer: PHARMACIA & UPJOHN COMPANY LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: TABLET
Routes: ORAL
Marketing started: 19811016
Marketing ended: 20261231
FDA application: NDA018276

## Active ingredients

- ALPRAZOLAM: 1 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0009-0090"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0009-0090
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=388e249d-b9b6-44c3-9f8f-880eced0239f