NDC 45963-678
metoprolol succinate 200 mg tablet, film coated, extended release
On the label: Actavis Pharma, Inc..
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
- 200 mg
- Approval
- ANDA ANDA204161
- On the market since
- Oct 23, 2019
- Package NDCs
45963-678-11- Official label
- DailyMed (National Library of Medicine), updated Dec 1, 2024
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