Labetalol Hydrochloride 70518-4201-00

Package NDC

70518-4201-00

Manufacturer: Remedyrepack Inc.
Dosage Form: Tablet, Film Coated
Route: Oral
Product Type: Human Prescription Drug
Marketing Start: October 2, 2024
Listing Expires: December 31, 2026
Application: ANDA075215

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Active Ingredients

Ingredient	Strength
Labetalol	100 mg/1

Drug Class

beta-Adrenergic Blocker [EPC]Adrenergic beta-Antagonists [MoA]beta-Adrenergic Blocker [EPC]

Selected Package

70518-4201-00Selected

180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4201-0)