NDC 36000-322 – Labetalol Hydrochloride

Labetalol Hydrochloride 5 mg/mL · Injection, Solution · Intravenous

Human Prescription Drug

Product NDC36000-322

Product details

Brand name
Labetalol Hydrochloride
Generic name
Labetalol Hydrochloride
Labeler
Baxter Healthcare Corporation
Dosage form
Injection, Solution
Route
Intravenous
Marketing category
ANDA · ANDA076051
Marketed since
January 26, 2021
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
36000-322-021 VIAL in 1 CARTON (36000-322-02) / 20 mL in 1 VIAL (36000-322-01)Jan 26, 2021

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