NDC 50090-6833 – Labetalol Hydrochloride

Labetalol Hydrochloride 300 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC50090-6833

Product details

Brand name
Labetalol Hydrochloride
Generic name
Labetalol Hydrochloride
Labeler
A-S Medication Solutions
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA075215
Marketed since
February 8, 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
50090-6833-190 TABLET, FILM COATED in 1 BOTTLE (50090-6833-1)Nov 21, 2023

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