Labetalol Hydrochloride 71335-2057-01

Package NDC

71335-2057-01

Product NDC: 71335-2057

Manufacturer: Bryant Ranch Prepack
Dosage Form: Tablet, Film Coated
Route: Oral
Product Type: Human Prescription Drug
Marketing Start: November 22, 2019
Listing Expires: December 31, 2027
Application: ANDA075215

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Active Ingredients

Ingredient	Strength
Labetalol	200 mg/1

Drug Class

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

Selected Package

71335-2057-01Selected

30 TABLET, FILM COATED in 1 BOTTLE (71335-2057-1)

Other packages for this product(2)

71335-2057-02

90 TABLET, FILM COATED in 1 BOTTLE (71335-2057-2)

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71335-2057-03

60 TABLET, FILM COATED in 1 BOTTLE (71335-2057-3)

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