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
- 63629-1523_fc6ec7d9-ec72-4ba7-929f-0460f00e71dc
- Product NDC
- 63629-1523
- 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 (63629-1523-0) · 63629-1523-0
- 12 TABLET in 1 BOTTLE (63629-1523-1) · 63629-1523-1
- 15 TABLET in 1 BOTTLE (63629-1523-2) · 63629-1523-2
- 20 TABLET in 1 BOTTLE (63629-1523-3) · 63629-1523-3
- 30 TABLET in 1 BOTTLE (63629-1523-4) · 63629-1523-4
- 60 TABLET in 1 BOTTLE (63629-1523-5) · 63629-1523-5
- 90 TABLET in 1 BOTTLE (63629-1523-6) · 63629-1523-6
- 10 TABLET in 1 BOTTLE (63629-1523-7) · 63629-1523-7
- 1 TABLET in 1 BOTTLE (63629-1523-9) · 63629-1523-9
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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