NDC 10135-712 – Labetalol Hydrochloride

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

Human Prescription Drug

Product NDC10135-712

Product details

Brand name
Labetalol Hydrochloride
Generic name
Labetalol
Labeler
Marlex Pharmaceuticals Inc
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA075215
Marketed since
October 1, 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 (2)

Package NDCDescriptionSince
10135-712-01100 TABLET, FILM COATED in 1 BOTTLE (10135-712-01)Oct 1, 2020
10135-712-05500 TABLET, FILM COATED in 1 BOTTLE (10135-712-05)Oct 1, 2020

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