NDC 43063-821 – Metoprolol Tartrate

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

Human Prescription Drug

Product NDC43063-821

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
Marketing end
August 31, 2027
Pharmacologic class
beta-Adrenergic Blocker

Active ingredients

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

Package NDC codes (4)

Package NDCDescriptionSince
43063-821-3030 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-821-30)Jun 27, 2018
43063-821-6060 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-821-60)May 17, 2018
43063-821-9090 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-821-90)Jan 5, 2017
43063-821-93180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-821-93)Jan 5, 2017

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