NDC 50742-617 – Metoprolol Succinate

Metoprolol Succinate 100 mg/1 · Tablet, Extended Release · Oral

Human Prescription Drug

Product NDC50742-617

Product details

Brand name
Metoprolol Succinate
Generic name
Metoprolol succinate
Labeler
Ingenus Pharmaceuticals, LLC
Dosage form
Tablet, Extended Release
Route
Oral
Marketing category
ANDA · ANDA204106
Marketed since
February 6, 2018
Listing expires
December 31, 2027
Pharmacologic class
beta-Adrenergic Blocker

Active ingredients

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

Package NDC codes (5)

Package NDCDescriptionSince
50742-617-01100 TABLET, EXTENDED RELEASE in 1 BOTTLE (50742-617-01)Feb 6, 2018
50742-617-05500 TABLET, EXTENDED RELEASE in 1 BOTTLE (50742-617-05)Feb 6, 2018
50742-617-101000 TABLET, EXTENDED RELEASE in 1 BOTTLE (50742-617-10)Feb 6, 2018
50742-617-9090 TABLET, EXTENDED RELEASE in 1 BOTTLE (50742-617-90)Feb 6, 2018
50742-617-9932362 TABLET, EXTENDED RELEASE in 1 DRUM (50742-617-99)Apr 9, 2021

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