NDC 71335-9749 – Metoprolol Succinate

Metoprolol Succinate 50 mg/1 · Tablet, Extended Release · Oral

Human Prescription Drug

Product NDC71335-9749

Product details

Brand name
Metoprolol Succinate
Generic name
Metoprolol succinate
Labeler
Bryant Ranch Prepack
Dosage form
Tablet, Extended Release
Route
Oral
Marketing category
ANDA · ANDA207465
Marketed since
March 25, 2019
Listing expires
December 31, 2026
Pharmacologic class
beta-Adrenergic Blocker

Active ingredients

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

Package NDC codes (7)

Package NDCDescriptionSince
71335-9749-130 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-9749-1)Jul 11, 2023
71335-9749-2100 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-9749-2)Jul 11, 2023
71335-9749-390 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-9749-3)Jul 11, 2023
71335-9749-4120 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-9749-4)Jul 11, 2023
71335-9749-560 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-9749-5)Jul 11, 2023
71335-9749-6180 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-9749-6)Jul 11, 2023
71335-9749-710 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-9749-7)Jul 11, 2023

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