Labetalol Hydrochloride

NDC 55154-0181 · Cardinal Health 107, LLC

Generic nameLabetalol Hydrochloride

Dosage formTABLET, FILM COATED

RouteORAL

Active ingredient(s)LABETALOL HYDROCHLORIDE

Strength100 mg/1

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

Marketing categoryANDA

Packages

55154-0181-0 — 10 BLISTER PACK in 1 BAG (55154-0181-0) / 1 TABLET, FILM COATED in 1 BLISTER PACK

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

50090-7523 — Labetalol Hydrochloride, 50090-7524 — Labetalol Hydrochloride, 50090-7666 — Labetalol Hydrochloride, 50090-7731 — Labetalol Hydrochloride, 50090-7743 — Labetalol Hydrochloride, 51407-614 — Labetalol Hydrochloride, 51407-615 — Labetalol Hydrochloride, 51407-616 — Labetalol Hydrochloride, 51655-322 — Labetalol Hydrochloride, 51662-1602 — LABETALOL HCl, 55154-0182 — Labetalol Hydrochloride, 55154-0184 — Labetalol Hydrochloride, 55154-2143 — Labetalol Hydrochloride, 55154-4747 — Labetalol Hydrochloride, 55154-8192 — Labetalol Hydrochloride, 60687-439 — Labetalol Hydrochloride, 60687-450 — Labetalol Hydrochloride, 60687-461 — Labetalol Hydrochloride, 60760-784 — Labetalol Hydrochloride, 60760-991 — 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.