NDC 68071-3941 – Metoprolol Tartrate

Metoprolol Tartrate 100 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC68071-3941

Product details

Brand name
Metoprolol Tartrate
Generic name
Metoprolol Tartrate
Labeler
NuCare 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
68071-3941-660 TABLET, FILM COATED in 1 BOTTLE (68071-3941-6)Jan 7, 2026

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