Labetalol Hydrochloride

NDC 71335-3065 · Bryant Ranch Prepack

Generic nameLabetalol Hydrochloride

Dosage formTABLET, FILM COATED

RouteORAL

Active ingredient(s)LABETALOL

Strength100 mg/1

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

Marketing categoryANDA

Packages

71335-3065-1 — 30 TABLET, FILM COATED in 1 BOTTLE (71335-3065-1)

71335-3065-2 — 90 TABLET, FILM COATED in 1 BOTTLE (71335-3065-2)

71335-3065-3 — 60 TABLET, FILM COATED in 1 BOTTLE (71335-3065-3)

71335-3065-4 — 120 TABLET, FILM COATED in 1 BOTTLE (71335-3065-4)

71335-3065-5 — 10 TABLET, FILM COATED in 1 BOTTLE (71335-3065-5)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

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, 71335-9690 — Labetalol Hydrochloride, 72162-1675 — Labetalol Hydrochloride, 72162-1676 — Labetalol Hydrochloride, 72162-1677 — 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.