NDC 0143-9623 – Labetalol Hydrochloride

Labetalol Hydrochloride 5 mg/mL · Injection · Intravenous

Human Prescription Drug

Product NDC0143-9623

Product details

Brand name
Labetalol Hydrochloride
Generic name
Labetalol Hydrochloride
Labeler
Hikma Pharmaceuticals USA Inc.
Dosage form
Injection
Route
Intravenous
Marketing category
ANDA · ANDA075303
Marketed since
November 29, 1999
Listing expires
December 31, 2026
Pharmacologic class
beta-Adrenergic Blocker

Active ingredients

Uses, dosage, side effects and warnings for Labetalol Hydrochloride →

Package NDC codes (1)

Package NDCDescriptionSince
0143-9623-011 VIAL in 1 BOX, UNIT-DOSE (0143-9623-01) / 40 mL in 1 VIALNov 29, 1999

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