NDC 70518-2868
Metoprolol Succinate 50 mg tablet, extended release
On the label: Remedyrepack Inc.. It's repackaged: Remedyrepack Inc. rebottles it from Cipla USA., Inc.'s NDC 69097-407.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| CTX Lifesciences Pvt. Ltd. | Surat, India | Makes the active ingredient | Problems found, fixed voluntarilySep 2, 2022 · 5 inspections, 1 with FDA action |
| Cipla Limited | Indore, India | Makes it, tests it, packages it and labels it | Serious problems, FDA actionFeb 17, 2023 · 6 inspections, 1 with FDA action |
| Moehs Catalana SL | Rubi, Spain | Makes the active ingredient | Problems found, fixed voluntarilyNov 10, 2023 · 6 inspections |
Product details
- Generic drug
- Metoprolol: every company that makes it
- Form
- tablet, extended release
- Strength
- 50 mg
- Approval
- ANDA ANDA207465
- On the market since
- Sep 6, 2020
- Package NDCs
70518-2868-070518-2868-170518-2868-2- Official label
- DailyMed (National Library of Medicine), updated Jul 11, 2025
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