NDC 71335-1878 – Metoprolol succinate

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

Human Prescription Drug

Product NDC71335-1878

Product details

Brand name
Metoprolol succinate
Generic name
Metoprolol succinate
Labeler
Bryant Ranch Prepack
Dosage form
Tablet, Extended Release
Route
Oral
Marketing category
ANDA · ANDA203894
Marketed since
June 7, 2018
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
71335-1878-130 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1878-1)Aug 17, 2021
71335-1878-2100 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1878-2)Sep 13, 2021
71335-1878-390 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1878-3)Jun 14, 2021
71335-1878-4120 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1878-4)Sep 19, 2022
71335-1878-560 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1878-5)Sep 19, 2022
71335-1878-6180 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1878-6)Sep 19, 2022
71335-1878-710 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1878-7)Sep 19, 2022

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