Labetalol Hydrochloride 33342-0516-15

Package NDC

33342-0516-15

Manufacturer: Macleods Pharmaceuticals Limited
Dosage Form: Tablet, Film Coated
Route: Oral
Product Type: Human Prescription Drug
Marketing Start: September 23, 2025
Listing Expires: December 31, 2026
Application: ANDA217949

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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

33342-0516-15Selected

500 TABLET, FILM COATED in 1 BOTTLE (33342-516-15)

Other packages for this product(1)

33342-0516-11

100 TABLET, FILM COATED in 1 BOTTLE (33342-516-11)

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