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
- 68682-655_0e23d654-d8b9-af1c-e063-6294a90a6f14
- Product NDC
- 68682-655
- Form
- GEL
- Composition / generic term
- Diazepam
- Labeler
- Oceanside Pharmaceuticals
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start / end (source format)
- 19970729
- Source listing expiry
- 20261231
Source-listed ingredients
- DIAZEPAM — 20 mg/4mL
These values do not establish equivalence or a dose recommendation.
Packages
- 2 SYRINGE, PLASTIC in 1 PACKAGE (68682-655-20) / 4 mL in 1 SYRINGE, PLASTIC · 68682-655-20
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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