Labetalol Hydrochloride 58657-0603-50

Package NDC

58657-0603-50

Manufacturer: Method Pharmaceuticals, Llc
Dosage Form: Tablet, Film Coated
Route: Oral
Product Type: Human Prescription Drug
Marketing Start: November 22, 2019
Listing Expires: December 31, 2026
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

58657-0603-50Selected

500 TABLET, FILM COATED in 1 BOTTLE (58657-603-50)

Other packages for this product(1)

58657-0603-01

100 TABLET, FILM COATED in 1 BOTTLE (58657-603-01)

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