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Labetalol Hydrochloride

NDC 72266-102 · Fosun Pharma USA Inc.

Generic nameLabetalol Hydrochloride
Dosage formINJECTION
RouteINTRAVENOUS
Active ingredient(s)LABETALOL HYDROCHLORIDE
Strength5 mg/mL
Pharmacologic classAdrenergic beta-Antagonists [MoA], beta-Adrenergic Blocker [EPC]
Marketing categoryANDA

Packages

72266-102-01 — 1 VIAL, MULTI-DOSE in 1 CARTON (72266-102-01) / 20 mL in 1 VIAL, MULTI-DOSE

Billed under HCPCS

J1920 — Injection, labetalol hydrochloride, 5 mg Medicare Part B payment limit (ASP + 6%): $0.22

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

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, 71335-2169 — Labetalol Hydrochloride, 71335-2434 — Labetalol Hydrochloride, 71335-2475 — Labetalol Hydrochloride, 72266-103 — Labetalol Hydrochloride, 72572-350 — Labetalol Hydrochloride, 72603-146 — Labetalol Hydrochloride, 72603-902 — Labetalol Hydrochloride, 72603-903 — Labetalol Hydrochloride, 72603-904 — Labetalol Hydrochloride, 72888-120 — Labetalol Hydrochloride, 72888-121 — Labetalol Hydrochloride, 72888-122 — Labetalol Hydrochloride, 72888-468 — 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.