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
- 71335-2306_b9906136-3102-42b2-9599-7109a9a41f0f
- Product NDC
- 71335-2306
- 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 — 10 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 56 TABLET in 1 BOTTLE, PLASTIC (71335-2306-0) · 71335-2306-0
- 20 TABLET in 1 BOTTLE, PLASTIC (71335-2306-1) · 71335-2306-1
- 30 TABLET in 1 BOTTLE, PLASTIC (71335-2306-2) · 71335-2306-2
- 40 TABLET in 1 BOTTLE, PLASTIC (71335-2306-3) · 71335-2306-3
- 50 TABLET in 1 BOTTLE, PLASTIC (71335-2306-4) · 71335-2306-4
- 60 TABLET in 1 BOTTLE, PLASTIC (71335-2306-5) · 71335-2306-5
- 90 TABLET in 1 BOTTLE, PLASTIC (71335-2306-6) · 71335-2306-6
- 100 TABLET in 1 BOTTLE, PLASTIC (71335-2306-7) · 71335-2306-7
- 10 TABLET in 1 BOTTLE, PLASTIC (71335-2306-8) · 71335-2306-8
- 120 TABLET in 1 BOTTLE, PLASTIC (71335-2306-9) · 71335-2306-9
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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