Labetalol Hydrochloride

NDC 10135-712 · Marlex Pharmaceuticals Inc

Generic nameLabetalol

Dosage formTABLET, FILM COATED

RouteORAL

Active ingredient(s)LABETALOL

Strength200 mg/1

Pharmacologic classAdrenergic beta-Antagonists [MoA], beta-Adrenergic Blocker [EPC]

Marketing categoryANDA

Packages

10135-712-01 — 100 TABLET, FILM COATED in 1 BOTTLE (10135-712-01)

10135-712-05 — 500 TABLET, FILM COATED in 1 BOTTLE (10135-712-05)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

10135-711 — Labetalol, 10135-713 — Labetalol, 58657-602 — Labetalol Hydrochloride, 58657-603 — Labetalol Hydrochloride, 58657-604 — Labetalol Hydrochloride, 58657-906 — Labetalol Hydrochloride, 58657-907 — Labetalol Hydrochloride, 58657-908 — Labetalol Hydrochloride, 63629-1161 — Labetalol Hydrochloride, 63629-1162 — Labetalol Hydrochloride, 63629-1163 — Labetalol Hydrochloride, 63629-1164 — Labetalol Hydrochloride, 63629-1165 — Labetalol Hydrochloride, 63629-1166 — Labetalol Hydrochloride, 70518-4201 — Labetalol Hydrochloride, 71335-2057 — Labetalol Hydrochloride, 71335-2876 — Labetalol Hydrochloride, 71335-2923 — Labetalol Hydrochloride, 71335-3065 — Labetalol Hydrochloride, 71335-9690 — Labetalol Hydrochloride, +3 more

From the FDA National Drug Code Directory, retrieved 2026-08-24. Product listings are submitted by labelers; FDA does not verify them.