Labetalol Hydrochloride 00409-2267

Product NDC

00409-2267

Manufacturer: Hospira, Inc.
Dosage Form: Injection, Solution
Route: Intravenous
Product Type: Human Prescription Drug
Marketing Start: December 30, 2005
Listing Expires: December 31, 2026
Application: ANDA075240

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Active Ingredients

Ingredient	Strength
Labetalol Hydrochloride	5 mg/mL

Drug Class

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

Packaging Options(1)

00409-2267-54

1 VIAL, MULTI-DOSE in 1 CARTON (0409-2267-54) / 40 mL in 1 VIAL, MULTI-DOSE

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