NDC 82009-113 – Metoprolol succinate

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

Human Prescription Drug

Product NDC82009-113

Product details

Brand name
Metoprolol succinate
Generic name
Metoprolol succinate
Labeler
Quallent Pharmaceuticals Health LLC
Dosage form
Tablet, Film Coated, Extended Release
Route
Oral
Marketing category
ANDA · ANDA090617
Marketed since
July 20, 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 (1)

Package NDCDescriptionSince
82009-113-05500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (82009-113-05)Jul 20, 2023

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