NDCFind

Labetalol Hydrochloride 51655-0322-25

Package NDC

51655-0322-25

Product NDC: 51655-0322

Manufacturer
Northwind Health Company, Llc
Dosage Form
Tablet, Film Coated
Route
Oral
Product Type
Human Prescription Drug
Marketing Start
April 25, 2023
Listing Expires
December 31, 2027
Application
ANDA209603
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Active Ingredients

IngredientStrength
Labetalol Hydrochloride100 mg/1

Drug Class

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

Selected Package

51655-0322-25Selected

60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-322-25)