NDC 0904-7082
Nifedipine 90 mg tablet, film coated, extended release
On the label: Major Pharmaceuticals. It's repackaged: Major Pharmaceuticals rebottles it from Ingenus Pharmaceuticals, LLC's NDC 50742-262.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Novast Laboratories Ltd. | Nantong, China | Makes it, tests it, packages it and labels it | Problems found, fixed voluntarilyJul 14, 2023 · 5 inspections |
Recalls
- Jul 2, 2021 · Class II · The Harvard Drug Group
Failed Dissolution Specification: Out of specification for dissolution during routine stability testing.
Lots: Lots: a)N00418 Exp. 09/2022, b) N00417 Exp. 09/2022
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Nifedipine: every company that makes it
- Form
- tablet, film coated, extended release, oral
- Strength
- 90 mg
- Approval
- ANDA ANDA210614
- On the market since
- Mar 12, 2019
- Package NDCs
0904-7082-040904-7082-06- Official label
- DailyMed (National Library of Medicine), updated Apr 30, 2026
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