NDC 71335-3167 – Metoprolol succinate

Metoprolol Succinate 100 mg/1 · Tablet, Extended Release · Oral

Human Prescription Drug

Product NDC71335-3167

Product details

Brand name
Metoprolol succinate
Generic name
Metoprolol succinate
Labeler
Bryant Ranch Prepack
Dosage form
Tablet, Extended Release
Route
Oral
Marketing category
ANDA · ANDA214110
Marketed since
July 21, 2025
Listing expires
December 31, 2027
Pharmacologic class
beta-Adrenergic Blocker

Active ingredients

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

Package NDC codes (7)

Package NDCDescriptionSince
71335-3167-130 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-3167-1)Aug 4, 2026
71335-3167-290 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-3167-2)Aug 4, 2026
71335-3167-3120 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-3167-3)Aug 4, 2026
71335-3167-420 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-3167-4)Aug 4, 2026
71335-3167-5100 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-3167-5)Aug 4, 2026
71335-3167-660 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-3167-6)Aug 4, 2026
71335-3167-710 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-3167-7)Aug 4, 2026

Other Metoprolol Succinate products