NDCFind

Labetalol Hydrochloride 58657-0602-01

Package NDC

58657-0602-01

Product NDC: 58657-0602

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

IngredientStrength
Labetalol100 mg/1

Drug Class

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

Selected Package

58657-0602-01Selected

100 TABLET, FILM COATED in 1 BOTTLE (58657-602-01)

Other packages for this product(1)

500 TABLET, FILM COATED in 1 BOTTLE (58657-602-50)