# Alprazolam

NDC: 80425-0284
Generic name: Alprazolam
Labeler / Manufacturer: Advanced Rx of Tennessee, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20230308
Marketing ended: 20270319
FDA application: ANDA074112

## Active ingredients

- ALPRAZOLAM: .5 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"80425-0284"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=80425-0284
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=f667458d-ddda-4e9e-e053-2995a90adb5a