NDC 58657-906 – Labetalol Hydrochloride

Labetalol 100 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC58657-906

Product details

Brand name
Labetalol Hydrochloride
Generic name
Labetalol Hydrochloride
Labeler
Method Pharmaceuticals, LLC
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA075215
Marketed since
July 1, 2025
Listing expires
December 31, 2026
Pharmacologic class
beta-Adrenergic Blocker

Active ingredients

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

Package NDC codes (1)

Package NDCDescriptionSince
58657-906-01100 BLISTER PACK in 1 CARTON (58657-906-01) / 1 TABLET, FILM COATED in 1 BLISTER PACK (58657-906-10)Jul 1, 2025

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