Labetalol hydrochloride

NDC 50090-6778 · A-S Medication Solutions

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

50090-6778-0 — 90 TABLET, FILM COATED in 1 BOTTLE (50090-6778-0)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

33342-517 — Labetalol Hydrochloride, 36000-320 — Labetalol Hydrochloride, 36000-322 — Labetalol Hydrochloride, 36000-324 — Labetalol Hydrochloride, 42806-327 — Labetalol Hydrochloride, 42806-328 — Labetalol Hydrochloride, 42806-329 — Labetalol Hydrochloride, 50090-1290 — Labetalol Hydrochloride, 50090-6741 — Labetalol Hydrochloride, 50090-6774 — Labetalol Hydrochloride, 50090-6833 — Labetalol Hydrochloride, 50090-7156 — Labetalol hydrochloride, 50090-7457 — Labetalol Hydrochloride, 50090-7458 — Labetalol Hydrochloride, 50090-7523 — Labetalol Hydrochloride, 50090-7524 — Labetalol Hydrochloride, 50090-7666 — Labetalol Hydrochloride, 50090-7731 — Labetalol Hydrochloride, 50090-7743 — Labetalol Hydrochloride, 51407-614 — 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.