United States · FDA National Drug Code directory
Midazolam In Sodium Chloride
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
- 65219-650_a43f63a4-8a7f-4a1b-b9a0-4198486cfef6
- Product NDC
- 65219-650
- Form
- INJECTION, SOLUTION
- Composition / generic term
- Midazolam In Sodium Chloride
- Labeler
- FRESENIUS KABI USA, LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20250115
- Source listing expiry
- 20261231
Source-listed ingredients
- MIDAZOLAM HYDROCHLORIDE — 1 mg/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 10 POUCH in 1 CARTON (65219-650-10) / 1 BAG in 1 POUCH / 100 mL in 1 BAG · 65219-650-10
- 10 POUCH in 1 CARTON (65219-650-50) / 1 BAG in 1 POUCH / 50 mL in 1 BAG · 65219-650-50
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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