NDC 42291-903
Sunitinib Malate 37.5 mg capsule
On the label: AvKARE, Inc.. It's repackaged: AvKARE, Inc. rebottles it from Teva Pharmaceuticals USA, Inc.'s NDC 0093-8229.
Where the pills inside were 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 Teva Pharmaceuticals USA, Inc. names for other drugs.
Recalls
- Oct 18, 2024 · Class II · AvKARE
Labeling: Label Mix-Up
Lots: Lot #: 100049371, Exp. Date 07/31/2026 - Oct 18, 2024 · Class II · AvKARE
Labeling: Label Mix-Up
Lots: Lot #: 100049501, Exp. Date 07/31/2026 - Jul 5, 2023 · Class II · Teva Pharmaceuticals USA Inc
Failed Moisture Limits: Water (moisture) content above the approved product specifications.
Lots: Lot # 100037220, Exp 10/2024
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Sunitinib: every company that makes it
- Form
- capsule, oral
- Strength
- 37.5 mg
- Approval
- ANDA ANDA213803
- On the market since
- Oct 11, 2023
- Package NDCs
42291-903-28- Official label
- DailyMed (National Library of Medicine), updated Jan 16, 2026
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