NDC 68071-2240
Carbidopa And Levodopa 25 mg / 100 mg tablet
On the label: NuCare Pharmaceuticals.Inc.. It's repackaged: NuCare Pharmaceuticals.Inc. rebottles it from Caraco Pharmaceutical Laboratories, Ltd.'s NDC 62756-518.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Sun Pharmaceutical Industries Limited | Halol, India | Makes it and tests it | Serious problems, FDA actionJun 13, 2025 · 12 inspections, 5 with FDA action |
Repackaging site
- NuCare Pharmaceuticals,Inc., Orange, CA, United States · relabels it
Recalls
- Jan 12, 2017 · Class II · Sun Pharmaceutical Industries, Inc.
Failed Dissolution Specifications
Lots: a) JKP5530A Exp. 12/17, JKP3991A Exp. 11/17, JKR6535A Exp. 07/18 b) JKP5529A Exp. 11/17
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Carbidopa and Levodopa: every company that makes it
- Form
- tablet, oral
- Strength
- 25 mg / 100 mg
- Approval
- ANDA ANDA078536
- On the market since
- Oct 28, 2008
- Package NDCs
68071-2240-1- Official label
- DailyMed (National Library of Medicine), updated Jul 17, 2024
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