NDC 63323-411 – Midazolam

Midazolam Hydrochloride 1 mg/mL · Injection, Solution · Intramuscular, Intravenous

Human Prescription Drug DEA schedule CIV 2 recalls

Product NDC63323-411

Product details

Brand name
Midazolam
Generic name
Midazolam Hydrochloride
Labeler
Fresenius Kabi USA, LLC
Dosage form
Injection, Solution
Route
Intramuscular, Intravenous
Marketing category
ANDA · ANDA075154
Marketed since
July 14, 2000
Listing expires
December 31, 2026
Pharmacologic class
Benzodiazepine

Active ingredients

Uses, dosage, side effects and warnings for Midazolam →

Package NDC codes (4)

Package NDCDescriptionSince
63323-411-1010 VIAL in 1 TRAY (63323-411-10) / 10 mL in 1 VIAL (63323-411-13)Jul 14, 2000
63323-411-1225 VIAL in 1 TRAY (63323-411-12) / 2 mL in 1 VIAL (63323-411-15)Jul 14, 2000
63323-411-2525 VIAL in 1 TRAY (63323-411-25) / 5 mL in 1 VIAL (63323-411-18)Jul 14, 2000
63323-411-2725 VIAL in 1 TRAY (63323-411-27) / 2 mL in 1 VIAL (63323-411-22)Jan 6, 2025

Recalls mentioning this NDC

Other Midazolam products