Labetalol Hydrochloride 00409-2339-34

Package NDC

00409-2339-34

Manufacturer: Hospira, Inc.
Dosage Form: Injection, Solution
Route: Intravenous
Product Type: Human Prescription Drug
Marketing Start: October 18, 2005
Listing Expires: December 31, 2026
Application: ANDA075239

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Active Ingredients

Ingredient	Strength
Labetalol Hydrochloride	5 mg/mL

Drug Class

Adrenergic beta-Antagonists [MoA]beta-Adrenergic Blocker [EPC]

Selected Package

00409-2339-34Selected

10 CARTON in 1 PACKAGE (0409-2339-34) / 1 CARTRIDGE in 1 CARTON / 4 mL in 1 CARTRIDGE (0409-2339-24)