NDC 71335-9706 – Metoprolol succinate

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

Human Prescription Drug

Product NDC71335-9706

Product details

Brand name
Metoprolol succinate
Generic name
Metoprolol succinate
Labeler
Bryant Ranch Prepack
Dosage form
Tablet, Extended Release
Route
Oral
Marketing category
ANDA · ANDA213854
Marketed since
April 29, 2021
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
71335-9706-130 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-9706-1)Jul 16, 2024
71335-9706-290 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-9706-2)Aug 16, 2023
71335-9706-3120 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-9706-3)Jul 16, 2024
71335-9706-420 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-9706-4)Jul 16, 2024
71335-9706-5100 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-9706-5)Jul 16, 2024
71335-9706-660 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-9706-6)Jul 16, 2024
71335-9706-710 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-9706-7)Jul 16, 2024

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