Labetalol Hydrochloride

NDC 68382-799 · Zydus Pharmaceuticals USA Inc.

Generic nameLabetalol Hydrochloride

Dosage formTABLET, FILM COATED

RouteORAL

Active ingredient(s)LABETALOL HYDROCHLORIDE

Strength200 mg/1

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

Marketing categoryANDA

Packages

68382-799-01 — 100 TABLET, FILM COATED in 1 BOTTLE (68382-799-01)

68382-799-05 — 500 TABLET, FILM COATED in 1 BOTTLE (68382-799-05)

68382-799-06 — 30 TABLET, FILM COATED in 1 BOTTLE (68382-799-06)

68382-799-16 — 90 TABLET, FILM COATED in 1 BOTTLE (68382-799-16)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

67296-2156 — Labetalol Hydrochloride, 68001-381 — Labetalol Hydrochloride, 68001-382 — Labetalol Hydrochloride, 68001-383 — Labetalol Hydrochloride, 68001-700 — Labetalol Hydrochloride, 68001-701 — Labetalol Hydrochloride, 68001-702 — Labetalol Hydrochloride, 68071-3878 — Labetalol Hydrochloride, 68083-111 — Labetalol Hydrochloride, 68382-798 — Labetalol Hydrochloride, 68382-800 — Labetalol Hydrochloride, 70121-2428 — labetalol hydrochloride, 70377-060 — Labetalol Hydrochloride, 70377-061 — Labetalol Hydrochloride, 70377-062 — Labetalol Hydrochloride, 70377-063 — Labetalol Hydrochloride, 70518-3499 — Labetalol Hydrochloride, 70518-3993 — Labetalol Hydrochloride, 70771-1163 — Labetalol Hydrochloride, 70771-1164 — Labetalol Hydrochloride, +99 more

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