NDC 82868-087
Metoprolol Succinate 25 mg tablet, film coated, extended release
On the label: Northwind Pharmaceuticals. It's repackaged: Northwind Pharmaceuticals rebottles it from Granules Pharmaceuticals Inc.'s NDC 70010-780.
Where the pills inside were 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 Granules Pharmaceuticals Inc. names for other drugs.
Repackaging site
- Northwind Health Company, LLC, Indianapolis, IN, United States · repackages it
Recalls
- Jun 24, 2025 · Class II · Granules Pharmaceuticals Inc.
Failed Dissolution Specifications: Product failed to meet dissolution acceptance criteria in the stability studies at the 6th month (25¿C/60% RH) long-term.
Lots: Lot # a)1400008A, Exp Date: 12/31/2025; b) 1400008B, Exp Date: 12/31/2025
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 ANDA216916
- On the market since
- Sep 15, 2025
- Package NDCs
82868-087-3082868-087-90- Official label
- DailyMed (National Library of Medicine), updated Jan 12, 2026
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