Labetalol Hydrochloride 72266-0103-41

Package NDC

72266-0103-41

Manufacturer: Fosun Pharma Usa Inc.
Dosage Form: Injection
Route: Intravenous
Product Type: Human Prescription Drug
Marketing Start: March 31, 2021
Listing Expires: December 31, 2026
Application: ANDA090699

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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

72266-0103-41Selected

1 VIAL, MULTI-DOSE in 1 CARTON (72266-103-41) / 40 mL in 1 VIAL, MULTI-DOSE