NDC 65862-062 – Metoprolol Tartrate

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

Human Prescription Drug 1 recall

Product NDC65862-062

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 (2)

Package NDCDescriptionSince
65862-062-01100 TABLET, FILM COATED in 1 BOTTLE (65862-062-01)Sep 11, 2007
65862-062-991000 TABLET, FILM COATED in 1 BOTTLE (65862-062-99)Sep 11, 2007

Recalls mentioning this NDC

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