NDC 76045-001 – Midazolam

Midazolam Hydrochloride 2 mg/2mL · Injection, Solution · Intramuscular, Intravenous

Human Prescription Drug DEA schedule CIV 1 recall

Product NDC76045-001

Product details

Brand name
Midazolam
Generic name
Midazolam Hydrochloride
Labeler
Fresenius Kabi USA, LLC
Dosage form
Injection, Solution
Route
Intramuscular, Intravenous
Marketing category
ANDA · ANDA203460
Marketed since
October 3, 2014
Listing expires
December 31, 2026
Pharmacologic class
Benzodiazepine

Active ingredients

Uses, dosage, side effects and warnings for Midazolam →

Package NDC codes (1)

Package NDCDescriptionSince
76045-001-2024 BLISTER PACK in 1 CARTON (76045-001-20) / 1 SYRINGE, GLASS in 1 BLISTER PACK (76045-001-00) / 2 mL in 1 SYRINGE, GLASSOct 3, 2014

Recalls mentioning this NDC

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