NDC 70518-4201 – Labetalol Hydrochloride

Labetalol 100 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC70518-4201

Product details

Brand name
Labetalol Hydrochloride
Generic name
Labetalol Hydrochloride
Labeler
REMEDYREPACK INC.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA075215
Marketed since
October 2, 2024
Listing expires
December 31, 2027
Pharmacologic class
beta-Adrenergic Blocker

Active ingredients

Uses, dosage, side effects and warnings for Labetalol Hydrochloride →

Package NDC codes (1)

Package NDCDescriptionSince
70518-4201-0180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4201-0)Oct 2, 2024

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