NDC 71335-0158 – Metoprolol succinate

Metoprolol Succinate 25 mg/1 · Tablet, Extended Release · Oral

Human Prescription Drug

Product NDC71335-0158

Product details

Brand name
Metoprolol succinate
Generic name
Metoprolol succinate
Labeler
Bryant Ranch Prepack
Dosage form
Tablet, Extended Release
Route
Oral
Marketing category
ANDA · ANDA090617
Marketed since
September 10, 2012
Listing expires
December 31, 2026
Pharmacologic class
beta-Adrenergic Blocker

Active ingredients

Uses, dosage, side effects and warnings for Metoprolol Succinate →

Package NDC codes (5)

Package NDCDescriptionSince
71335-0158-1100 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-0158-1)Jun 27, 2013
71335-0158-230 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-0158-2)Jun 27, 2013
71335-0158-390 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-0158-3)Jun 27, 2013
71335-0158-4120 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-0158-4)Jun 27, 2013
71335-0158-560 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-0158-5)Jun 27, 2013

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