NDC 54458-950
Nifedipine 30 mg tablet, extended release
On the label: International Laboratories, LLC.
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Lannett Company, LLC | Seymour, IN, United States | Makes it | Problems found, fixed voluntarilyOct 21, 2022 · 9 inspections, 1 with FDA action |
| International Laboratories, LLC | Seminole, Florida, United States | Repackages it and relabels it | Problems found, fixed voluntarilyApr 23, 2015 · 2 inspections |
Product details
- Generic drug
- Nifedipine: every company that makes it
- Form
- tablet, extended release
- Strength
- 30 mg
- Approval
- ANDA ANDA077127
- On the market since
- Aug 21, 2009
- Package NDCs
54458-950-10- Official label
- DailyMed (National Library of Medicine), updated Jun 9, 2017
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