NDC 60687-402 – Metoprolol Succinate

Metoprolol Succinate 50 mg/1 · Tablet, Film Coated, Extended Release · Oral

Human Prescription Drug

Product NDC60687-402

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 · ANDA090617
Marketed since
December 7, 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 (2)

Package NDCDescriptionSince
60687-402-01100 BLISTER PACK in 1 CARTON (60687-402-01) / 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (60687-402-11)Dec 7, 2018
60687-402-6550 BLISTER PACK in 1 CARTON (60687-402-65) / 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (60687-402-11)Mar 8, 2023

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