NDC 0143-9533
Allopurinol sodium 500 mg per 25 mL injection, powder, lyophilized, for solution
On the label: Hikma Pharmaceuticals USA Inc..
Where it's 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 Hikma Pharmaceuticals USA Inc. names for other drugs.
Product details
- Generic drug
- Allopurinol: every company that makes it
- Form
- injection, powder, lyophilized, for solution, intravenous
- Strength
- 500 mg per 25 mL
- Approval
- ANDA ANDA076870
- On the market since
- Sep 1, 2004
- Package NDCs
0143-9533-01- Official label
- DailyMed (National Library of Medicine), updated Mar 1, 2022
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