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
- 71335-2133_8ea1648d-8205-4d5f-af0c-b77772d049db
- Product NDC
- 71335-2133
- Form
- TABLET
- Composition / generic term
- Alprazolam
- Labeler
- Bryant Ranch Prepack
- Marketing category
- ANDA
- Marketing start / end (source format)
- 19931001
- Source listing expiry
- 20261231
Source-listed ingredients
- ALPRAZOLAM — .25 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 10 TABLET in 1 BOTTLE (71335-2133-0) · 71335-2133-0
- 30 TABLET in 1 BOTTLE (71335-2133-1) · 71335-2133-1
- 100 TABLET in 1 BOTTLE (71335-2133-2) · 71335-2133-2
- 60 TABLET in 1 BOTTLE (71335-2133-3) · 71335-2133-3
- 20 TABLET in 1 BOTTLE (71335-2133-4) · 71335-2133-4
- 90 TABLET in 1 BOTTLE (71335-2133-5) · 71335-2133-5
- 15 TABLET in 1 BOTTLE (71335-2133-6) · 71335-2133-6
- 120 TABLET in 1 BOTTLE (71335-2133-7) · 71335-2133-7
- 40 TABLET in 1 BOTTLE (71335-2133-8) · 71335-2133-8
- 14 TABLET in 1 BOTTLE (71335-2133-9) · 71335-2133-9
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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