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
- 0172-3926_db225e5f-9265-4460-ab58-3305246c6258
- Product NDC
- 0172-3926
- Form
- TABLET
- Composition / generic term
- Diazepam
- Labeler
- Teva Pharmaceuticals USA, Inc.
- 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
- 100 TABLET in 1 BOTTLE (0172-3926-60) · 0172-3926-60
- 500 TABLET in 1 BOTTLE (0172-3926-70) · 0172-3926-70
- 1000 TABLET in 1 BOTTLE (0172-3926-80) · 0172-3926-80
Source and coverage
Open FDA National Drug Code directory →
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.
Browse United States records →