NDC 0781-3528
Cyclophosphamide 500 mg per 5 mL injection, solution, concentrate
On the label: Sandoz 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 Sandoz Inc. names for other drugs.
Recalls
- Sep 5, 2025 · Class II · Sandoz Inc
cGMP deviations: Temperature excursion during transportation.
Lots: Only the following 6 GTN Numbers for Lot # 110459 exp. date 02/28/2027: (01)00307813528104(21)10686040629319 (01)00307813528104(21)10687281435306 (01)00307813528104(21)10687409963168 (01)00307813528104(21)10701200331212 (01)00307813528104(21)10687325644911 (01)00307813528104(21)1068766116…
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- 4-Hydroxycyclophosphamide: every company that makes it
- Form
- injection, solution, concentrate, intravenous
- Strength
- 500 mg per 5 mL
- Approval
- NDA NDA217150
- On the market since
- Apr 8, 2024
- Package NDCs
0781-3528-100781-3528-75- Official label
- DailyMed (National Library of Medicine), updated Dec 30, 2024
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