NDC 71335-0167 – Metoprolol succinate

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

Human Prescription Drug

Product NDC71335-0167

Product details

Brand name
Metoprolol succinate
Generic name
Metoprolol succinate
Labeler
Bryant Ranch Prepack
Dosage form
Tablet, Film Coated, Extended Release
Route
Oral
Marketing category
ANDA · ANDA078889
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 (7)

Package NDCDescriptionSince
71335-0167-130 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-0167-1)Feb 12, 2018
71335-0167-290 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-0167-2)Feb 16, 2018
71335-0167-3120 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-0167-3)Feb 14, 2018
71335-0167-420 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-0167-4)May 2, 2022
71335-0167-5100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-0167-5)May 2, 2022
71335-0167-660 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-0167-6)May 2, 2022
71335-0167-710 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-0167-7)May 2, 2022

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