NDC 70518-3993 – Labetalol Hydrochloride

Labetalol Hydrochloride 200 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC70518-3993

Product details

Brand name
Labetalol Hydrochloride
Generic name
Labetalol Hydrochloride
Labeler
REMEDYREPACK INC.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA209603
Marketed since
January 24, 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 (3)

Package NDCDescriptionSince
70518-3993-090 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3993-0)Jan 24, 2024
70518-3993-1180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3993-1)Jan 24, 2024
70518-3993-2180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3993-2)Jan 20, 2025

Other Labetalol Hydrochloride products