NDC 71205-724 – Metoprolol Succinate

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

Human Prescription Drug

Product NDC71205-724

Product details

Brand name
Metoprolol Succinate
Generic name
Metoprolol Succinate
Labeler
Proficient Rx LP
Dosage form
Tablet, Film Coated, Extended Release
Route
Oral
Marketing category
ANDA · ANDA205541
Marketed since
November 6, 2020
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
71205-724-3030 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71205-724-30)Nov 17, 2022
71205-724-6060 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71205-724-60)Nov 17, 2022
71205-724-9090 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71205-724-90)Nov 17, 2022

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