NDCFind

Labetalol Hydrochloride 68001-0381-03

Package NDC

68001-0381-03

Product NDC: 68001-0381

Manufacturer
Bluepoint Laboratories Inc.
Dosage Form
Tablet, Film Coated
Route
Oral
Product Type
Human Prescription Drug
Marketing Start
February 18, 2019
Listing Expires
December 31, 2026
Application
ANDA207743
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Active Ingredients

IngredientStrength
Labetalol Hydrochloride100 mg/1

Drug Class

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

Selected Package

68001-0381-03Selected

500 TABLET, FILM COATED in 1 BOTTLE (68001-381-03)

Other packages for this product(1)

100 TABLET, FILM COATED in 1 BOTTLE (68001-381-00)