Labetalol Hydrochloride

NDC 0904-7452 · Major Pharmaceuticals

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

0904-7452-61 — 100 BLISTER PACK in 1 CARTON (0904-7452-61) / 1 TABLET, FILM COATED in 1 BLISTER PACK

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

0143-9365 — LABETALOL HYDROCHLORIDE, 0143-9366 — Labetalol Hydrochloride, 0143-9622 — Labetalol Hydrochloride, 0143-9623 — Labetalol Hydrochloride, 0409-0125 — Labetalol Hydrochloride, 0409-2339 — Labetalol Hydrochloride, 0591-0605 — Labetalol hydrochloride, 0615-8512 — Labetalol Hydrochloride, 0615-8513 — Labetalol Hydrochloride, 0904-7451 — Labetalol Hydrochloride, 0904-7453 — Labetalol Hydrochloride, 23155-723 — Labetalol Hydrochloride, 23155-724 — Labetalol Hydrochloride, 23155-725 — Labetalol Hydrochloride, 23155-726 — Labetalol Hydrochloride, 25021-317 — labetalol hydrochloride, 29300-252 — Labetalol Hydrochloride, 29300-253 — Labetalol Hydrochloride, 29300-254 — Labetalol Hydrochloride, 33342-515 — 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.