NDC 71205-368 – Metoprolol succinate

Metoprolol Succinate 25 mg/1 · Tablet, Film Coated, Extended Release · Oral

Human Prescription Drug

Product NDC71205-368

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 · ANDA204161
Marketed since
October 23, 2019
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
71205-368-3030 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71205-368-30)Dec 3, 2019
71205-368-6060 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71205-368-60)Dec 3, 2019
71205-368-9090 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71205-368-90)Dec 3, 2019

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