NDC 25021-830
zoledronic acid 0.05 mg per 1 mL injection, solution
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
- Mar 4, 2014 · Class II · Sagent Pharmaceuticals Inc
Lack of Assurance of Sterility; leaking of premix bags
Lots: NDC 25021-830-82; Lot Numbers and Expiration Dates: Lot 30076, Expires 01/2015; Lot 30077, Expires 01/2015.
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Zoledronic Acid: every company that makes it
- Form
- injection, solution, intravenous
- Strength
- 0.05 mg per 1 mL
- Approval
- ANDA ANDA202828
- On the market since
- Mar 2, 2013
- Package NDCs
25021-830-8225021-830-87- Official label
- DailyMed (National Library of Medicine), updated Jul 14, 2026
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