Labetalol Hydrochloride 60687-0450-01

Package NDC

60687-0450-01

Manufacturer: American Health Packaging
Dosage Form: Tablet, Film Coated
Route: Oral
Product Type: Human Prescription Drug
Marketing Start: July 16, 2019
Listing Expires: December 31, 2026
Application: ANDA207743

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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

60687-0450-01Selected

100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-450-01) / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-450-11)