NDC 25021-317 – Labetalol hydrochloride

Labetalol Hydrochloride 5 mg/mL · Injection, Solution · Intravenous

Human Prescription Drug

Product NDC25021-317

Product details

Brand name
Labetalol hydrochloride
Generic name
Labetalol hydrochloride
Labeler
Sagent Pharmaceuticals
Dosage form
Injection, Solution
Route
Intravenous
Marketing category
ANDA · ANDA214533
Marketed since
September 1, 2022
Listing expires
December 31, 2026
Pharmacologic class
beta-Adrenergic Blocker

Active ingredients

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

Package NDC codes (2)

Package NDCDescriptionSince
25021-317-201 VIAL in 1 CARTON (25021-317-20) / 20 mL in 1 VIALSep 1, 2022
25021-317-401 VIAL in 1 CARTON (25021-317-40) / 40 mL in 1 VIALSep 1, 2022

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