United States · FDA National Drug Code directory
Triazolam
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
- 71335-1876_4087c69a-e64e-4f97-a7dc-c7b2ec02f64b
- Product NDC
- 71335-1876
- Form
- TABLET
- Composition / generic term
- Triazolam
- Labeler
- Bryant Ranch Prepack
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20201020
- Source listing expiry
- 20261231
Source-listed ingredients
- TRIAZOLAM — .25 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 3 TABLET in 1 BOTTLE, PLASTIC (71335-1876-0) · 71335-1876-0
- 10 TABLET in 1 BOTTLE, PLASTIC (71335-1876-1) · 71335-1876-1
- 30 TABLET in 1 BOTTLE, PLASTIC (71335-1876-2) · 71335-1876-2
- 60 TABLET in 1 BOTTLE, PLASTIC (71335-1876-3) · 71335-1876-3
- 40 TABLET in 1 BOTTLE, PLASTIC (71335-1876-4) · 71335-1876-4
- 90 TABLET in 1 BOTTLE, PLASTIC (71335-1876-5) · 71335-1876-5
- 6 TABLET in 1 BOTTLE, PLASTIC (71335-1876-6) · 71335-1876-6
- 1 TABLET in 1 BOTTLE, PLASTIC (71335-1876-7) · 71335-1876-7
- 2 TABLET in 1 BOTTLE, PLASTIC (71335-1876-8) · 71335-1876-8
- 28 TABLET in 1 BOTTLE, PLASTIC (71335-1876-9) · 71335-1876-9
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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