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Labetalol Hydrochloride

NDC 71247-130 · Innogenix, Inc.

Generic nameLabetalol Hydrochloride

Dosage formTABLET, FILM COATED

RouteORAL

Active ingredient(s)LABETALOL HYDROCHLORIDE

Strength300 mg/1

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

Marketing categoryANDA

Packages

71247-130-01 — 100 TABLET, FILM COATED in 1 BOTTLE (71247-130-01)

71247-130-05 — 500 TABLET, FILM COATED in 1 BOTTLE (71247-130-05)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

70518-3993 — Labetalol Hydrochloride, 70771-1163 — Labetalol Hydrochloride, 70771-1164 — Labetalol Hydrochloride, 70771-1165 — Labetalol Hydrochloride, 71205-095 — Labetalol hydrochloride, 71209-083 — Labetalol Hydrochloride, 71209-084 — Labetalol Hydrochloride, 71209-085 — Labetalol Hydrochloride, 71247-126 — Labetalol Hydrochloride, 71247-127 — Labetalol Hydrochloride, 71335-1242 — Labetalol Hydrochloride, 71335-1410 — Labetalol Hydrochloride, 71335-2063 — Labetalol Hydrochloride, 71335-2145 — Labetalol Hydrochloride, 71335-2169 — Labetalol Hydrochloride, 71335-2434 — Labetalol Hydrochloride, 71335-2475 — Labetalol Hydrochloride, 72266-102 — Labetalol Hydrochloride, 72266-103 — Labetalol Hydrochloride, 72572-350 — Labetalol Hydrochloride, +99 more

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