NDC 68462-121
Nicardipine Hydrochloride 30 mg capsule
On the label: Glenmark Pharmaceuticals Inc., USA.
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Glenmark Pharmaceuticals Limited | Dhar, India | Makes it and packages it | Serious problems, FDA actionFeb 14, 2025 · 8 inspections, 1 with FDA action |
Product details
- Generic drug
- Nicardipine: every company that makes it
- Form
- capsule, oral
- Strength
- 30 mg
- Approval
- ANDA ANDA216357
- On the market since
- Dec 16, 2022
- Package NDCs
68462-121-0568462-121-90- Official label
- DailyMed (National Library of Medicine), updated Jan 29, 2026
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