Novitium Pharma LLC
East Windsor, NJ, United States · makes it, tests it, packages it and labels it
No problems found Last FDA inspection Feb 16, 2024. 5 inspections on record.
NDC 51655-403
Digoxin 0.125 mg tablet
On the label: Northwind Pharmaceuticals.
It's a repackaged product: Northwind Pharmaceuticals rebottles it from ANI Pharmaceuticals, Inc.'s NDC 70954-201.
Where the pills inside were made
Repackaging site
- Northwind Health Company, LLC, Indianapolis, IN, United States · repackages it
Recalls
- Mar 25, 2024 · Class III · Terminated
Failed Impurities/Degradation Specifications
Lots: Lot M23011A; Exp. 12/2024 - Mar 4, 2024 · Class III · Terminated
Cross Contamination with Other Products:(mycophenolate mofetil).
Lots: Lot #: M23172A, Exp 01/31/2025
Product details
- Generic drug
- Digoxin: see every company that makes it
- Form
- tablet, oral
- Strength
- 0.125 mg
- Approval
- ANDA ANDA215307
- On the market since
- Apr 13, 2023
- Package NDCs
51655-403-52- Official label
- DailyMed (National Library of Medicine), updated Jan 1, 2026
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