NDC 68788-8869 – Metoprolol Succinate

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

Human Prescription Drug

Product NDC68788-8869

Product details

Brand name
Metoprolol Succinate
Generic name
Metoprolol Succinate
Labeler
Preferred Pharmaceuticals Inc.
Dosage form
Tablet, Film Coated, Extended Release
Route
Oral
Marketing category
ANDA · ANDA216916
Marketed since
April 30, 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 (3)

Package NDCDescriptionSince
68788-8869-330 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68788-8869-3)Apr 30, 2025
68788-8869-660 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68788-8869-6)Apr 30, 2025
68788-8869-990 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68788-8869-9)Apr 30, 2025

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