NDC 71205-162 – Metoprolol Succinate

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

Human Prescription Drug

Product NDC71205-162

Product details

Brand name
Metoprolol Succinate
Generic name
Metoprolol succinate
Labeler
Proficient Rx LP
Dosage form
Tablet, Extended Release
Route
Oral
Marketing category
NDA AUTHORIZED GENERIC · NDA019962
Marketed since
January 1, 2018
Listing expires
December 31, 2026
Pharmacologic class
beta-Adrenergic Blocker

Active ingredients

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

Package NDC codes (3)

Package NDCDescriptionSince
71205-162-3030 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-162-30)Nov 1, 2018
71205-162-6060 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-162-60)Nov 1, 2018
71205-162-9090 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-162-90)Nov 1, 2018

Other Metoprolol Succinate products