NDC 0409-2339 – Labetalol Hydrochloride

Labetalol Hydrochloride 5 mg/mL · Injection, Solution · Intravenous

Human Prescription Drug 1 recall

Product NDC0409-2339

Product details

Brand name
Labetalol Hydrochloride
Generic name
Labetalol Hydrochloride
Labeler
Hospira, Inc.
Dosage form
Injection, Solution
Route
Intravenous
Marketing category
ANDA · ANDA075239
Marketed since
October 18, 2005
Listing expires
December 31, 2026
Pharmacologic class
beta-Adrenergic Blocker

Active ingredients

Uses, dosage, side effects and warnings for Labetalol Hydrochloride →

Package NDC codes (1)

Package NDCDescriptionSince
0409-2339-3410 CARTON in 1 PACKAGE (0409-2339-34) / 1 CARTRIDGE in 1 CARTON / 4 mL in 1 CARTRIDGE (0409-2339-24)Oct 18, 2005

Recalls mentioning this NDC

Other Labetalol Hydrochloride products