metoprolol succinate 25 mg tablet, film coated, extended release

Where it's made

This label doesn't name the factory that makes the drug. Companies don't have to print it on the label. The maker's name is often on the stock bottle your pharmacy used; you can ask the pharmacist. See the plants Actavis Pharma, Inc. names for other drugs.

Recalls

• Jan 29, 2026 · Class II · Teva Pharmaceuticals USA, Inc
  Failed Dissolution Specifications
  Lots: Lot#: a) 0715J251, Exp.: 12/2026; 0716J251, Exp.: 01/2027; 0717J251, Exp.: 01/2027; b) 0715J252, Exp.: 12/2026; 0716J252, Exp.: 01/2027, 0717J252, Exp.: 01/2027.
• Jan 29, 2026 · Class II · Teva Pharmaceuticals USA, Inc
  Failed Dissolution Specifications
  Lots: Lot#: a) 0486G251, 0487G251, 0488G251, Exp.: 01/2027; b) 0486G252, 0487G253, 0488G252, Exp.: 01/2027.
• Jan 29, 2026 · Class II · Teva Pharmaceuticals USA, Inc
  Failed Dissolution Specifications
  Lots: Lot#: a) 0718J251, 0729J251, 0730J251, Exp.: 12/2026; b) 0718J252, 0729J252, 0730J252, Exp.: 12/2026.
• Jan 29, 2026 · Class II · Teva Pharmaceuticals USA, Inc
  Failed Dissolution Specifications
  Lots: Lot#: a) 0686H251, 0687H251, 10688H251, Exp.: 02/2027. .
• Jan 26, 2022 · Class II · Cardinal Healthcare
  CGMP Deviations: Products were exposed to temperatures outside of the products labeled storage conditions.
  Lots: Batch 2447J211

Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.

Product details

Generic drug

Metoprolol: every company that makes it

Form

tablet, film coated, extended release, oral

Strength

25 mg

Approval

ANDA ANDA204161

On the market since

Oct 23, 2019

Package NDCs

45963-709-11 45963-709-96

Official label

DailyMed (National Library of Medicine), updated Dec 1, 2024

Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?