Labetalol Hydrochloride 70377-0063-11

Package NDC

70377-0063-11

Manufacturer: Biocon Pharma Inc.
Dosage Form: Tablet, Film Coated
Route: Oral
Product Type: Human Prescription Drug
Marketing Start: December 2, 2024
Listing Expires: December 31, 2027
Application: ANDA209603

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Active Ingredients

Ingredient	Strength
Labetalol Hydrochloride	400 mg/1

Drug Class

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

Selected Package

70377-0063-11Selected

30 TABLET, FILM COATED in 1 BOTTLE (70377-063-11)

Other packages for this product(2)

70377-0063-12

100 TABLET, FILM COATED in 1 BOTTLE (70377-063-12)

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70377-0063-13

500 TABLET, FILM COATED in 1 BOTTLE (70377-063-13)

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