NDC 72789-583 – Metoprolol Tartrate

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

Human Prescription Drug

Product NDC72789-583

Product details

Brand name
Metoprolol Tartrate
Generic name
Metoprolol tartrate
Labeler
PD-Rx Pharmaceuticals, Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA076704
Marketed since
December 23, 1993
Listing expires
December 31, 2027
Pharmacologic class
beta-Adrenergic Blocker

Active ingredients

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

Package NDC codes (3)

Package NDCDescriptionSince
72789-583-3030 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-583-30)Aug 5, 2026
72789-583-6060 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-583-60)Jul 28, 2026
72789-583-9090 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-583-90)Aug 11, 2026

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