NDC 42291-421
Leflunomide 20 mg tablet
On the label: AvKARE, Inc.. It's repackaged: AvKARE, Inc. rebottles it from Apotex Corp.'s NDC 60505-2503.
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 Apotex Corp. names for other drugs.
Recalls
- Jun 14, 2007 · Class II · Apotex Corp.
Subpotent (Single Ingredient Drug): Distribution of product that did not meet specifications.
Lots: Lot #: GZ1274, Exp 11/07.
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Leflunomide: every company that makes it
- Form
- tablet, oral
- Strength
- 20 mg
- Approval
- ANDA ANDA077090
- On the market since
- Jun 13, 2019
- Package NDCs
42291-421-30- Official label
- DailyMed (National Library of Medicine), updated Jan 14, 2026
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?