United States · FDA National Drug Code directory

Metoprolol succinate

A source-listed medicine record.

Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.

Medicine identity

Source reference
42806-727_2c74614f-0615-6839-e063-6294a90acc19
Product NDC
42806-727
Form
TABLET, EXTENDED RELEASE
Composition / generic term
Metoprolol succinate
Labeler
Epic Pharma, LLC
Marketing category
ANDA
Marketing start / end (source format)
20250201
Source listing expiry
20261231

Source-listed ingredients

  • METOPROLOL SUCCINATE — 200 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (42806-727-01) · 42806-727-01
  • 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (42806-727-05) · 42806-727-05
  • 1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (42806-727-10) · 42806-727-10

Source and coverage

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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.

Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.

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