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
- 71335-1584_dc33c03b-c55f-4b37-9b2b-85c949d2a1c3
- Product NDC
- 71335-1584
- Form
- TABLET
- Composition / generic term
- Diazepam
- Labeler
- Bryant Ranch Prepack
- Marketing category
- ANDA
- Marketing start / end (source format)
- 19861210
- 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 (71335-1584-0) · 71335-1584-0
- 12 TABLET in 1 BOTTLE (71335-1584-1) · 71335-1584-1
- 15 TABLET in 1 BOTTLE (71335-1584-2) · 71335-1584-2
- 20 TABLET in 1 BOTTLE (71335-1584-3) · 71335-1584-3
- 30 TABLET in 1 BOTTLE (71335-1584-4) · 71335-1584-4
- 60 TABLET in 1 BOTTLE (71335-1584-5) · 71335-1584-5
- 90 TABLET in 1 BOTTLE (71335-1584-6) · 71335-1584-6
- 10 TABLET in 1 BOTTLE (71335-1584-7) · 71335-1584-7
- 2 TABLET in 1 BOTTLE (71335-1584-8) · 71335-1584-8
- 1 TABLET in 1 BOTTLE (71335-1584-9) · 71335-1584-9
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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