NDC 67296-2115
Nifedipine 30 mg tablet, extended release
On the label: RedPharm Drug. Inc.. It's repackaged: RedPharm Drug. Inc. 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
- RedPharm Drug, Eden Prairie, MN, United States · repackages it
Product details
- Generic drug
- Nifedipine: every company that makes it
- Form
- tablet, extended release
- Strength
- 30 mg
- Approval
- ANDA ANDA075269
- On the market since
- Oct 18, 2012
- Package NDCs
67296-2115-3- Official label
- DailyMed (National Library of Medicine), updated Jul 25, 2024
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?