Labetalol hydrochloride

NDC 71205-095 · Proficient Rx LP

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

71205-095-30 — 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-095-30)

71205-095-60 — 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-095-60)

71205-095-90 — 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-095-90)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

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, 70771-1165 — Labetalol Hydrochloride, 71209-083 — Labetalol Hydrochloride, 71209-084 — Labetalol Hydrochloride, 71209-085 — Labetalol Hydrochloride, 71247-126 — Labetalol Hydrochloride, 71247-127 — Labetalol Hydrochloride, 71247-130 — Labetalol Hydrochloride, 71335-1242 — Labetalol Hydrochloride, 71335-1410 — Labetalol Hydrochloride, 71335-2063 — Labetalol Hydrochloride, 71335-2145 — 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.