NDC 71335-1951 – metoprolol succinate

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

Human Prescription Drug

Product NDC71335-1951

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
71335-1951-130 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1951-1)Dec 17, 2021
71335-1951-290 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1951-2)Sep 14, 2021
71335-1951-3120 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1951-3)Sep 19, 2022
71335-1951-420 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1951-4)Sep 19, 2022
71335-1951-5100 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1951-5)Sep 19, 2022
71335-1951-660 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1951-6)Oct 13, 2021
71335-1951-710 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1951-7)Sep 19, 2022

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