NDC 82868-084 – Metoprolol Succinate

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

Human Prescription Drug

Product NDC82868-084

Product details

Brand name
Metoprolol Succinate
Generic name
Metoprolol Succinate
Labeler
Northwind Health Company, LLC
Dosage form
Tablet, Film Coated, Extended Release
Route
Oral
Marketing category
ANDA · ANDA216916
Marketed since
June 25, 2025
Listing expires
December 31, 2026
Pharmacologic class
beta-Adrenergic Blocker

Active ingredients

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

Package NDC codes (2)

Package NDCDescriptionSince
82868-084-3030 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (82868-084-30)Aug 26, 2025
82868-084-9090 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (82868-084-90)Jun 25, 2025

Other Metoprolol Succinate products