NDC 31722-589 – Metoprolol Succinate

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

Human Prescription Drug

Product NDC31722-589

Product details

Brand name
Metoprolol Succinate
Generic name
Metoprolol Succinate
Labeler
Camber Pharmaceuticals, Inc.
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 (4)

Package NDCDescriptionSince
31722-589-01100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (31722-589-01)Nov 6, 2020
31722-589-05500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (31722-589-05)Apr 23, 2021
31722-589-101000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (31722-589-10)Apr 23, 2021
31722-589-3030 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (31722-589-30)Nov 6, 2020

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