NDC 60687-413 – Metoprolol Succinate

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

Human Prescription Drug

Product NDC60687-413

Product details

Brand name
Metoprolol Succinate
Generic name
Metoprolol Succinate
Labeler
American Health Packaging
Dosage form
Tablet, Film Coated, Extended Release
Route
Oral
Marketing category
ANDA · ANDA078889
Marketed since
March 15, 2019
Listing expires
December 31, 2027
Pharmacologic class
beta-Adrenergic Blocker

Active ingredients

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

Package NDC codes (2)

Package NDCDescriptionSince
60687-413-01100 BLISTER PACK in 1 CARTON (60687-413-01) / 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (60687-413-11)Mar 15, 2019
60687-413-6550 BLISTER PACK in 1 CARTON (60687-413-65) / 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (60687-413-11)Mar 8, 2023

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