NDC 68084-597
Nifedipine 30 mg tablet, film coated, extended release
On the label: American Health Packaging. It's repackaged: American Health Packaging rebottles it from Lannett Company, Inc.'s NDC 62175-260.
Where the pills inside were made
This label doesn't name the factory that makes the drug. Companies don't have to print it on the label. The maker's name is often on the stock bottle your pharmacy used; you can ask the pharmacist. See the plants Lannett Company, Inc. names for other drugs.
Repackaging site
- American Health Packaging, Columbus, OH, United States · repackages it
Product details
- Generic drug
- Nifedipine: every company that makes it
- Form
- tablet, film coated, extended release, oral
- Strength
- 30 mg
- Approval
- ANDA ANDA077127
- On the market since
- Jun 13, 2012
- Package NDCs
68084-597-0168084-597-1168084-597-65- Official label
- DailyMed (National Library of Medicine), updated May 16, 2025
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