NDC 51655-281
Metoprolol Tartrate 50 mg tablet, film coated
On the label: Northwind Pharmaceuticals. It's repackaged: Northwind Pharmaceuticals rebottles it from TruPharma LLC.'s NDC 52817-361.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Rubicon Research Limited | Thane, India | Makes it | No problems foundMar 8, 2024 · 5 inspections |
Repackaging site
- Northwind Health Company, LLC, Indianapolis, IN, United States · repackages it
Recalls
- May 6, 2024 · Class II · Rubicon Research Private Limited
Presence of Foreign Substance: metal in tablet
Lots: Lot 231037H1, exp 6/2027 - Dec 31, 2021 · Class II · Rubicon Research Private Limited
Complaint received of foreign matter (metal) embedded in tablet.
Lots: Batch # 210211H1, Exp. date FEB 2024
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, oral
- Strength
- 50 mg
- Approval
- ANDA ANDA200981
- On the market since
- May 11, 2022
- Package NDCs
51655-281-25- Official label
- DailyMed (National Library of Medicine), updated Jan 1, 2026
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?