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
- 27808-303_a7845f10-48d0-478b-a760-c1fd208c09b9
- Product NDC
- 27808-303
- Form
- TABLET, EXTENDED RELEASE
- Composition / generic term
- Metoprolol Succinate
- Labeler
- Cranbury Pharmaceuticals, LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20250601
- Source listing expiry
- 20261231
Source-listed ingredients
- METOPROLOL SUCCINATE — 50 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (27808-303-01) · 27808-303-01
- 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (27808-303-02) · 27808-303-02
- 1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (27808-303-03) · 27808-303-03
Source and coverage
Open FDA National Drug Code directory →
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.
Browse United States records →