NDC 55111-466 – Metoprolol succinate

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

Human Prescription Drug 2 recalls

Product NDC55111-466

Product details

Brand name
Metoprolol succinate
Generic name
Metoprolol succinate
Labeler
Dr. Reddy's Laboratories Limited
Dosage form
Tablet, Film Coated, Extended Release
Route
Oral
Marketing category
ANDA · ANDA090617
Marketed since
September 10, 2012
Listing expires
December 31, 2026
Pharmacologic class
beta-Adrenergic Blocker

Active ingredients

Uses, dosage, side effects and warnings for Metoprolol Succinate →

Package NDC codes (5)

Package NDCDescriptionSince
55111-466-01100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (55111-466-01)Sep 10, 2012
55111-466-05500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (55111-466-05)Sep 10, 2012
55111-466-3030 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (55111-466-30)Sep 10, 2012
55111-466-6060 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (55111-466-60)Sep 10, 2012
55111-466-7810 BLISTER PACK in 1 CARTON (55111-466-78) / 10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (55111-466-79)Sep 10, 2012

Recalls mentioning this NDC

Other Metoprolol Succinate products