NDC 52817-360 – Metoprolol Tartrate

Metoprolol Tartrate 25 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug 2 recalls

Product NDC52817-360

Product details

Brand name
Metoprolol Tartrate
Generic name
Metoprolol Tartrate
Labeler
TruPharma LLC
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA200981
Marketed since
December 1, 2018
Listing expires
December 31, 2026
Pharmacologic class
beta-Adrenergic Blocker

Active ingredients

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

Package NDC codes (2)

Package NDCDescriptionSince
52817-360-001000 TABLET, FILM COATED in 1 BOTTLE (52817-360-00)Dec 1, 2018
52817-360-10 sample100 TABLET, FILM COATED in 1 BOTTLE (52817-360-10)Dec 1, 2018

Recalls mentioning this NDC

Other Metoprolol Tartrate products