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
- 50090-1913_8b32cbef-f70b-4b28-b267-9768b7a40197
- Product NDC
- 50090-1913
- Form
- TABLET
- Composition / generic term
- Diazepam
- Labeler
- A-S Medication Solutions
- 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
- 20 TABLET in 1 BOTTLE (50090-1913-1) · 50090-1913-1
- 30 TABLET in 1 BOTTLE (50090-1913-2) · 50090-1913-2
- 10 TABLET in 1 BOTTLE (50090-1913-4) · 50090-1913-4
- 100 TABLET in 1 BOTTLE (50090-1913-5) · 50090-1913-5
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 →