NDC 65862-063 – Metoprolol Tartrate

Metoprolol Tartrate 50 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug 1 recall

Product NDC65862-063

Product details

Brand name
Metoprolol Tartrate
Generic name
Metoprolol Tartrate
Labeler
Aurobindo Pharma Limited
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA077739
Marketed since
September 11, 2007
Listing expires
December 31, 2026
Pharmacologic class
beta-Adrenergic Blocker

Active ingredients

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

Package NDC codes (3)

Package NDCDescriptionSince
65862-063-01100 TABLET, FILM COATED in 1 BOTTLE (65862-063-01)Sep 11, 2007
65862-063-6060 TABLET, FILM COATED in 1 BOTTLE (65862-063-60)Sep 11, 2007
65862-063-991000 TABLET, FILM COATED in 1 BOTTLE (65862-063-99)Sep 11, 2007

Recalls mentioning this NDC

Other Metoprolol Tartrate products