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
- 61919-906_47e14ab4-5eb5-67c7-e063-6394a90a1e4b
- Product NDC
- 61919-906
- Form
- TABLET
- Composition / generic term
- DIAZEPAM
- Labeler
- Direct_Rx
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20161101
- Source listing expiry
- 20271231
Source-listed ingredients
- DIAZEPAM — 10 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 2 TABLET in 1 BOTTLE (61919-906-02) · 61919-906-02
- 5 TABLET in 1 BOTTLE (61919-906-05) · 61919-906-05
- 10 TABLET in 1 BOTTLE (61919-906-10) · 61919-906-10
- 30 TABLET in 1 BOTTLE (61919-906-30) · 61919-906-30
- 60 TABLET in 1 BOTTLE (61919-906-60) · 61919-906-60
- 90 TABLET in 1 BOTTLE (61919-906-90) · 61919-906-90
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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