Labetalol Hydrochloride 00143-9320-01

Package NDC

00143-9320-01

Manufacturer: Hikma Pharmaceuticals Usa Inc.
Dosage Form: Injection
Route: Intravenous
Product Type: Human Prescription Drug
Marketing Start: November 29, 1999
Listing Expires: December 31, 2026
Application: ANDA075303

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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

00143-9320-01Selected

1 VIAL in 1 BOX, UNIT-DOSE (0143-9320-01) / 20 mL in 1 VIAL