United States · FDA National Drug Code directory
Midazolam
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
- 63323-411_9814447b-a93e-42ad-b57e-5db0a5b7f552
- Product NDC
- 63323-411
- Form
- INJECTION, SOLUTION
- Composition / generic term
- MIDAZOLAM HYDROCHLORIDE
- Labeler
- Fresenius Kabi USA, LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20000714
- Source listing expiry
- 20261231
Source-listed ingredients
- MIDAZOLAM HYDROCHLORIDE — 1 mg/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 10 VIAL in 1 TRAY (63323-411-10) / 10 mL in 1 VIAL (63323-411-13) · 63323-411-10
- 25 VIAL in 1 TRAY (63323-411-12) / 2 mL in 1 VIAL (63323-411-15) · 63323-411-12
- 25 VIAL in 1 TRAY (63323-411-25) / 5 mL in 1 VIAL (63323-411-18) · 63323-411-25
- 25 VIAL in 1 TRAY (63323-411-27) / 2 mL in 1 VIAL (63323-411-22) · 63323-411-27
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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