NDC 68071-4097
Nifedipine 90 mg tablet, extended release
On the label: NuCare Pharmaceuticals.Inc.. It's repackaged: NuCare Pharmaceuticals.Inc. rebottles it from Upsher-Smith Laboratories, Inc.'s NDC 24979-009.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Bora Pharmaceutical Laboratories Inc. | Zhunan Township, Taiwan | Makes it and packages it | Problems found, fixed voluntarilyJul 21, 2025 · 7 inspections |
| Bora Pharmaceutical Laboratories Inc. Zhongli Plant | Taoyuan City, Taiwan | Makes it and tests it | Problems found, fixed voluntarilyFeb 7, 2020 · 4 inspections |
| Apace Packaging LLC | Fountain Run, KY, United States | Packages it | No problems foundJan 13, 2022 · 6 inspections |
Repackaging site
- NuCare Pharmaceuticals,Inc., Orange, CA, United States · repackages it
Product details
- Generic drug
- Nifedipine: every company that makes it
- Form
- tablet, extended release, oral
- Strength
- 90 mg
- Approval
- ANDA ANDA203126
- On the market since
- Nov 1, 2014
- Package NDCs
68071-4097-3- Official label
- DailyMed (National Library of Medicine), updated Jul 18, 2024
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