NDC 25021-241
Busulfan 6 mg per 1 mL injection, solution, concentrate
On the label: Sagent Pharmaceuticals.
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 Sagent Pharmaceuticals names for other drugs.
Recalls
- May 4, 2026 · Class III · Sagent Pharmaceuticals
Failed Impurities/Degradation Specifications
Lots: Lot #: 656412, Exp. Date 08/31/2026; 659646, Exp. Date 03/31/2027.
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Busulfan: every company that makes it
- Form
- injection, solution, concentrate, intravenous
- Strength
- 6 mg per 1 mL
- Approval
- ANDA ANDA207050
- On the market since
- May 15, 2017
- Package NDCs
25021-241-10- Official label
- DailyMed (National Library of Medicine), updated Jul 29, 2026
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