NDC 67296-1284
Warfarin Sodium 3 mg tablet
On the label: RedPharm Drug. Inc.. It's repackaged: RedPharm Drug. Inc. rebottles it from Teva Pharmaceuticals USA, Inc.'s NDC 0093-1715.
Where the pills inside were made
This label doesn't name the factory that makes the drug. Companies don't have to print it on the label. The maker's name is often on the stock bottle your pharmacy used; you can ask the pharmacist. See the plants Teva Pharmaceuticals USA, Inc. names for other drugs.
Repackaging site
- RedPharm Drug, Eden Prairie, MN, United States · repackages it
Recalls
- Jan 26, 2022 · Class II · Cardinal Healthcare
CGMP Deviations: Products were exposed to temperatures outside of the products labeled storage conditions.
Lots: Batch 2169041 - Jan 26, 2022 · Class II · Cardinal Healthcare
CGMP Deviations: Products were exposed to temperatures outside of the products labeled storage conditions.
Lots: Batch 2323041
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
- 3 mg
- Approval
- ANDA ANDA040616
- On the market since
- Jul 14, 2015
- Package NDCs
67296-1284-9- Official label
- DailyMed (National Library of Medicine), updated Jan 20, 2022
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