NDC 59923-714
Irinotecan Hydrochloride 20 mg per 1 mL injection
On the label: Areva Pharmaceuticals, 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 Areva Pharmaceuticals, Inc. names for other drugs.
Recalls
- Nov 19, 2020 · Class II · Areva Pharmaceuticals Inc
CGMP Deviations: based on a Warning Letter received by the manufacturer of the recalled product for inadequate out-of specification investigations, complaint and the investigation conclusions.
Lots: Lot 7S10022A, Exp Jan-21
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Irinotecan: every company that makes it
- Form
- injection
- Strength
- 20 mg per 1 mL
- Approval
- ANDA ANDA208718
- On the market since
- Mar 1, 2019
- Package NDCs
59923-714-02- Official label
- DailyMed (National Library of Medicine), updated Jan 14, 2021
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