NDC 51655-782
Allopurinol 300 mg tablet
On the label: Northwind Pharmaceuticals. It's repackaged: Northwind Pharmaceuticals rebottles it from Dr.Reddy's Laboratories Ltd.'s NDC 55111-730.
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 Dr.Reddy's Laboratories Ltd. names for other drugs.
Repackaging site
- Northwind Health Company, LLC, Indianapolis, IN, United States · repackages it
Recalls
- Jun 7, 2024 · Class II · Dr. Reddy's Laboratories, Inc.
Presence of foreign substance.
Lots: L2300594 - Jan 26, 2022 · Class II · Cardinal Healthcare
CGMP Deviations: Products were exposed to temperatures outside of the products labeled storage conditions.
Lots: Batch L100813
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Allopurinol: every company that makes it
- Form
- tablet, oral
- Strength
- 300 mg
- Approval
- ANDA ANDA071587
- On the market since
- Aug 4, 2021
- Package NDCs
51655-782-2651655-782-52- Official label
- DailyMed (National Library of Medicine), updated Jan 1, 2026
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