United States · FDA National Drug Code directory
Midazolam hydrochloride
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
- 23155-601_e20feff9-3aca-4bc1-a5c3-44fff8a9459c
- Product NDC
- 23155-601
- Form
- INJECTION, SOLUTION
- Composition / generic term
- Midazolam hydrochloride
- Labeler
- Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20161107
- Source listing expiry
- 20261231
Source-listed ingredients
- MIDAZOLAM HYDROCHLORIDE — 5 mg/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 10 VIAL, MULTI-DOSE in 1 CARTON (23155-601-41) / 5 mL in 1 VIAL, MULTI-DOSE (23155-601-31) · 23155-601-41
- 10 VIAL, MULTI-DOSE in 1 CARTON (23155-601-42) / 10 mL in 1 VIAL, MULTI-DOSE (23155-601-32) · 23155-601-42
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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