NDC 72266-102 – Labetalol Hydrochloride

Labetalol Hydrochloride 5 mg/mL · Injection · Intravenous

Human Prescription Drug

Product NDC72266-102

Product details

Brand name
Labetalol Hydrochloride
Generic name
Labetalol Hydrochloride
Labeler
Fosun Pharma USA Inc.
Dosage form
Injection
Route
Intravenous
Marketing category
ANDA · ANDA090699
Marketed since
April 2, 2019
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
72266-102-011 VIAL, MULTI-DOSE in 1 CARTON (72266-102-01) / 20 mL in 1 VIAL, MULTI-DOSEApr 2, 2019

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