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
- 43066-123_a0813073-d0b0-4fd7-b307-56f69c910c82
- Product NDC
- 43066-123
- Form
- INJECTION, SOLUTION
- Composition / generic term
- diazepam
- Labeler
- Baxter Healthcare Corporation
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20260728
- Source listing expiry
- 20271231
Source-listed ingredients
- DIAZEPAM — 20 mg/4mL
These values do not establish equivalence or a dose recommendation.
Packages
- 10 CARTON in 1 CARTON (43066-123-10) / 1 SYRINGE, PLASTIC in 1 CARTON (43066-123-01) / 4 mL in 1 SYRINGE, PLASTIC · 43066-123-10
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 →