NDC 70010-781 – Metoprolol Succinate

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

Human Prescription Drug 1 recall

Product NDC70010-781

Product details

Brand name
Metoprolol Succinate
Generic name
Metoprolol Succinate
Labeler
Granules Pharmaceuticals Inc.
Dosage form
Tablet, Film Coated, Extended Release
Route
Oral
Marketing category
ANDA · ANDA216916
Marketed since
October 2, 2023
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
70010-781-01100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (70010-781-01)Oct 2, 2023
70010-781-05500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (70010-781-05)Oct 2, 2023
70010-781-101000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (70010-781-10)Oct 2, 2023

Recalls mentioning this NDC

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