NDC 72789-535 – Metoprolol Tartrate

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

Human Prescription Drug

Product NDC72789-535

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 · ANDA077739
Marketed since
September 11, 2007
Listing expires
December 31, 2027
Pharmacologic class
beta-Adrenergic Blocker

Active ingredients

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

Package NDC codes (1)

Package NDCDescriptionSince
72789-535-9090 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-535-90)Nov 19, 2025

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