NDC 50268-541 – Metoprolol succinate

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

Human Prescription Drug

Product NDC50268-541

Product details

Brand name
Metoprolol succinate
Generic name
Metoprolol succinate
Labeler
AvPAK
Dosage form
Tablet, Film Coated, Extended Release
Route
Oral
Marketing category
ANDA · ANDA090617
Marketed since
July 25, 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 (1)

Package NDCDescriptionSince
50268-541-1550 BLISTER PACK in 1 BOX, UNIT-DOSE (50268-541-15) / 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (50268-541-11)Jul 25, 2018

Other Metoprolol Succinate products