# Alprazolam

NDC: 55289-523
Generic name: Alprazolam
Labeler / Manufacturer: PD-Rx Pharmaceuticals, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 19980325
Marketing ended: 20270319
FDA application: ANDA074909

## Active ingredients

- ALPRAZOLAM: 2 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"55289-523"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=55289-523
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=7538d0d0-346e-4c3e-8f7a-c1cac8ec8ed3