NDC 68382-567 – Metoprolol succinate

Metoprolol Succinate 200 mg/1 · Tablet, Extended Release · Oral

Human Prescription Drug

Product NDC68382-567

Product details

Brand name
Metoprolol succinate
Generic name
Metoprolol succinate
Labeler
Zydus Pharmaceuticals (USA) Inc.
Dosage form
Tablet, Extended Release
Route
Oral
Marketing category
ANDA · ANDA203894
Marketed since
June 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 (3)

Package NDCDescriptionSince
68382-567-01100 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-567-01)Jun 7, 2018
68382-567-05500 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-567-05)Jun 7, 2018
68382-567-101000 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-567-10)Jun 7, 2018

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