NDC 68682-108
nifedipine 30 mg tablet, film coated, extended release
On the label: Oceanside Pharmaceuticals..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Bausch Health Companies Inc. | Steinbach, Canada | Makes it | No problems foundMay 19, 2023 · 6 inspections |
Product details
- Generic drug
- Nifedipine: every company that makes it
- Form
- tablet, film coated, extended release, oral
- Strength
- 30 mg
- Approval
- ANDA ANDA075289
- On the market since
- Sep 27, 2000
- Package NDCs
68682-108-1068682-108-30- Official label
- DailyMed (National Library of Medicine), updated Feb 9, 2026
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