Labetalol Hydrochloride 00904-7453-61

Package NDC

00904-7453-61

Manufacturer: Major Pharmaceuticals
Dosage Form: Tablet, Film Coated
Route: Oral
Product Type: Human Prescription Drug
Marketing Start: October 8, 2024
Listing Expires: December 31, 2027
Application: ANDA209603

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Active Ingredients

Ingredient	Strength
Labetalol Hydrochloride	300 mg/1

Drug Class

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

Selected Package

00904-7453-61Selected

100 BLISTER PACK in 1 CARTON (0904-7453-61) / 1 TABLET, FILM COATED in 1 BLISTER PACK