NDC 27808-305 – Metoprolol Succinate

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

Human Prescription Drug

Product NDC27808-305

Product details

Brand name
Metoprolol Succinate
Generic name
Metoprolol Succinate
Labeler
Cranbury Pharmaceuticals, LLC
Dosage form
Tablet, Extended Release
Route
Oral
Marketing category
ANDA · ANDA207206
Marketed since
June 1, 2025
Listing expires
December 31, 2026
Pharmacologic class
beta-Adrenergic Blocker

Active ingredients

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

Package NDC codes (1)

Package NDCDescriptionSince
27808-305-01100 TABLET, EXTENDED RELEASE in 1 BOTTLE (27808-305-01)Jun 1, 2025

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