Labetalol Hydrochloride

NDC 68001-702 · BluePoint Laboratories

Generic nameLabetalol Hydrochloride

Dosage formTABLET

RouteORAL

Active ingredient(s)LABETALOL HYDROCHLORIDE

Strength300 mg/1

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

Marketing categoryANDA

Packages

68001-702-00 — 100 TABLET in 1 BOTTLE (68001-702-00)

68001-702-03 — 500 TABLET in 1 BOTTLE (68001-702-03)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

62135-800 — Labetalol Hydrochloride, 65145-124 — Labetalol Hydrochloride, 65145-125 — Labetalol Hydrochloride, 67296-2114 — Labetalol Hydrochloride, 67296-2156 — Labetalol Hydrochloride, 68001-381 — Labetalol Hydrochloride, 68001-382 — Labetalol Hydrochloride, 68001-383 — Labetalol Hydrochloride, 68001-700 — Labetalol Hydrochloride, 68001-701 — Labetalol Hydrochloride, 68071-3878 — Labetalol Hydrochloride, 68083-111 — Labetalol Hydrochloride, 68382-798 — Labetalol Hydrochloride, 68382-799 — Labetalol Hydrochloride, 68382-800 — Labetalol Hydrochloride, 70121-2428 — labetalol hydrochloride, 70377-060 — Labetalol Hydrochloride, 70377-061 — Labetalol Hydrochloride, 70377-062 — Labetalol Hydrochloride, 70377-063 — 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.