NDC 70882-133
Metoprolol Tartrate 50 mg tablet, film coated
On the label: Cambridge Therapeutics Technologies, LLC. It's repackaged: Cambridge Therapeutics Technologies, LLC rebottles it from Aurobindo Pharma Limited's NDC 65862-063.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Aurobindo Pharma Limited | Medchal, India | Makes it and tests it | Problems found, fixed voluntarilyJul 21, 2023 · 13 inspections, 1 with FDA action |
| Aurolife Pharma LLC | Dayton, NJ, United States | Makes it and tests it | Serious problems, FDA actionDec 7, 2021 · 10 inspections, 1 with FDA action |
Recalls
- Sep 9, 2021 · Class II · Aurobindo Pharma USA Inc.
Presence of Foreign Substance: Product complaints received for the presence of metal wire in one tablet.
Lots: Lot: MJ1019025-A, Exp. date 04/2022
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
- Strength
- 50 mg
- Approval
- ANDA ANDA077739
- On the market since
- Sep 11, 2007
- Package NDCs
70882-133-60- Official label
- DailyMed (National Library of Medicine), updated Oct 25, 2017
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