NDC 70377-063 – Labetalol Hydrochloride

Labetalol Hydrochloride 400 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC70377-063

Product details

Brand name
Labetalol Hydrochloride
Generic name
Labetalol Hydrochloride
Labeler
Biocon Pharma Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA209603
Marketed since
December 2, 2024
Listing expires
December 31, 2027
Pharmacologic class
beta-Adrenergic Blocker

Active ingredients

Uses, dosage, side effects and warnings for Labetalol Hydrochloride →

Package NDC codes (3)

Package NDCDescriptionSince
70377-063-1130 TABLET, FILM COATED in 1 BOTTLE (70377-063-11)Aug 7, 2025
70377-063-12100 TABLET, FILM COATED in 1 BOTTLE (70377-063-12)Dec 2, 2024
70377-063-13500 TABLET, FILM COATED in 1 BOTTLE (70377-063-13)Dec 2, 2024

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