Labetalol Hydrochloride 70518-3993-00

Package NDC

70518-3993-00

Manufacturer: Remedyrepack Inc.
Dosage Form: Tablet, Film Coated
Route: Oral
Product Type: Human Prescription Drug
Marketing Start: January 24, 2024
Listing Expires: December 31, 2026
Application: ANDA209603

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Active Ingredients

Ingredient	Strength
Labetalol Hydrochloride	200 mg/1

Drug Class

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

Selected Package

70518-3993-00Selected

90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3993-0)

Other packages for this product(2)

70518-3993-01

180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3993-1)

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70518-3993-02

180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3993-2)

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