NDC 67296-2156 – Labetalol Hydrochloride

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

Human Prescription Drug

Product NDC67296-2156

Product details

Brand name
Labetalol Hydrochloride
Generic name
Labetalol Hydrochloride
Labeler
Redpharm Drug
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA211953
Marketed since
August 18, 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
67296-2156-115 TABLET, FILM COATED in 1 BOTTLE (67296-2156-1)Aug 18, 2021

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