NDC 62135-800 – Labetalol Hydrochloride

Labetalol Hydrochloride 300 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC62135-800

Product details

Brand name
Labetalol Hydrochloride
Generic name
Labetalol Hydrochloride
Labeler
Chartwell RX, LLC
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA074787
Marketed since
February 22, 2020
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
62135-800-6060 TABLET in 1 BOTTLE (62135-800-60)Oct 24, 2023

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