NDC 60505-6236
Deferoxamine mesylate 500 mg injection, powder, lyophilized, for solution
On the label: Apotex Corp..
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 Apotex Corp. names for other drugs.
Product details
- Generic drug
- Deferoxamine: every company that makes it
- Form
- injection, powder, lyophilized, for solution, intramuscular; intravenous; subcutaneous
- Strength
- 500 mg
- Approval
- ANDA ANDA207384
- On the market since
- Nov 5, 2021
- Package NDCs
60505-6236-6- Official label
- DailyMed (National Library of Medicine), updated May 29, 2026
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?