Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Lupin Limited | Nagpur, India | Makes it and packages it | Problems found, fixed voluntarilyJul 11, 2023 · 4 inspections |
Recalls
- Nov 22, 2023 · Class II · Lupin Pharmaceuticals Inc.
Failed Dissolution Specifications
Lots: Lot # M200498, Exp. June 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
- Penicillamine: every company that makes it
- Form
- tablet, oral
- Strength
- 250 mg
- Approval
- ANDA ANDA212933
- On the market since
- Mar 1, 2021
- Package NDCs
70748-153-01- Official label
- DailyMed (National Library of Medicine), updated Dec 28, 2022
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