Labetalol Hydrochloride 50090-6778-00

Package NDC

50090-6778-00

Manufacturer: A-S Medication Solutions
Dosage Form: Tablet, Film Coated
Route: Oral
Product Type: Human Prescription Drug
Marketing Start: August 3, 1998
Listing Expires: December 31, 2026
Application: ANDA075133

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Active Ingredients

Ingredient	Strength
Labetalol Hydrochloride	200 mg/1

Drug Class

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

Selected Package

50090-6778-00Selected

90 TABLET, FILM COATED in 1 BOTTLE (50090-6778-0)