United States · FDA National Drug Code directory
Diazepam
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
- 71335-2239_a4623d8d-0257-43db-bd8a-be652068231a
- Product NDC
- 71335-2239
- Form
- TABLET
- Composition / generic term
- diazepam
- Labeler
- Bryant Ranch Prepack
- Marketing category
- ANDA
- Marketing start / end (source format)
- 19850904
- Source listing expiry
- 20261231
Source-listed ingredients
- DIAZEPAM — 5 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 120 TABLET in 1 BOTTLE, PLASTIC (71335-2239-0) · 71335-2239-0
- 12 TABLET in 1 BOTTLE, PLASTIC (71335-2239-1) · 71335-2239-1
- 15 TABLET in 1 BOTTLE, PLASTIC (71335-2239-2) · 71335-2239-2
- 20 TABLET in 1 BOTTLE, PLASTIC (71335-2239-3) · 71335-2239-3
- 30 TABLET in 1 BOTTLE, PLASTIC (71335-2239-4) · 71335-2239-4
- 60 TABLET in 1 BOTTLE, PLASTIC (71335-2239-5) · 71335-2239-5
- 90 TABLET in 1 BOTTLE, PLASTIC (71335-2239-6) · 71335-2239-6
- 10 TABLET in 1 BOTTLE, PLASTIC (71335-2239-7) · 71335-2239-7
- 2 TABLET in 1 BOTTLE, PLASTIC (71335-2239-8) · 71335-2239-8
- 1 TABLET in 1 BOTTLE, PLASTIC (71335-2239-9) · 71335-2239-9
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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