NDC 68071-4880 – Metoprolol Tartrate

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

Human Prescription Drug

Product NDC68071-4880

Product details

Brand name
Metoprolol Tartrate
Generic name
Metoprolol Tartrate
Labeler
NuCare Pharmaceuticals,Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA200981
Marketed since
December 1, 2018
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
68071-4880-1120 TABLET, FILM COATED in 1 BOTTLE (68071-4880-1)May 2, 2019
68071-4880-990 TABLET, FILM COATED in 1 BOTTLE (68071-4880-9)May 2, 2019

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