United States · FDA National Drug Code directory
Alprazolam
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 70954-510_18a6f29f-7eb8-4aa2-8121-d554c59da191
- Product NDC
- 70954-510
- Form
- TABLET
- Composition / generic term
- Alprazolam
- Labeler
- ANI Pharmaceuticals, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20210511
- Source listing expiry
- 20261231
Source-listed ingredients
- ALPRAZOLAM — 1 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET in 1 BOTTLE (70954-510-10) · 70954-510-10
- 500 TABLET in 1 BOTTLE (70954-510-20) · 70954-510-20
- 1000 TABLET in 1 BOTTLE (70954-510-30) · 70954-510-30
Source and coverage
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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
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