NDC 0591-0605 – Labetalol hydrochloride

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

Human Prescription Drug

Product NDC0591-0605

Product details

Brand name
Labetalol hydrochloride
Generic name
Labetalol hydrochloride
Labeler
Actavis Pharma, Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA075133
Marketed since
August 3, 1998
Marketing end
September 30, 2026
Pharmacologic class
beta-Adrenergic Blocker

Active ingredients

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

Package NDC codes (2)

Package NDCDescriptionSince
0591-0605-01100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0591-0605-01)Aug 3, 1998
0591-0605-05500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0591-0605-05)Aug 3, 1998

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