NDC 51655-798
Nifedipine 30 mg tablet, extended release
On the label: Northwind Pharmaceuticals. It's repackaged: Northwind Pharmaceuticals rebottles it from Oceanside Pharmaceuticals.'s NDC 68682-105.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Bausch Health Companies Inc. | Steinbach, Canada | Makes it | No problems foundMay 19, 2023 · 6 inspections |
Repackaging site
- Northwind Health Company, LLC, Indianapolis, IN, United States · repackages it
Product details
- Generic drug
- Nifedipine: every company that makes it
- Form
- tablet, extended release, oral
- Strength
- 30 mg
- Approval
- ANDA ANDA075269
- On the market since
- Feb 18, 2022
- Package NDCs
51655-798-26- Official label
- DailyMed (National Library of Medicine), updated Jan 1, 2026
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