NDC 51138-055
Warfarin Sodium 2 mg tablet
On the label: Med Health Pharma, LLC. It's repackaged: Med Health Pharma, LLC rebottles it from Caraco Pharmaceutical Laboratories, Ltd.'s NDC 51672-4028.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Taro Pharmaceutical Industries Ltd. | Haifa Bay, Israel | Makes it | No problems foundDec 8, 2022 · 7 inspections |
Recalls
- Aug 25, 2014 · Class III · Taro Pharmaceuticals U.S.A., Inc.
Failed Content Uniformity Specifications.
Lots: Lot #: 149400, Expiry: January 2016; Lot #: 149649, Expiry: January 2016.
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Warfarin: every company that makes it
- Form
- tablet
- Strength
- 2 mg
- Approval
- ANDA ANDA040301
- On the market since
- Feb 9, 2011
- Package NDCs
51138-055-30- Official label
- DailyMed (National Library of Medicine), updated Jan 20, 2012
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