NDC 66993-472
Nisoldipine 8.5 mg tablet, film coated, extended release
On the label: Prasco Laboratories.
Where it's 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 Prasco Laboratories names for other drugs.
Recalls
- Jul 24, 2015 · Class III · Shionogi Inc.
Failed Dissolution Specifications
Lots: Lot #: a) 8803472, Exp 03/16; b) 8803473, Exp 03/16
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Nisoldipine: every company that makes it
- Form
- tablet, film coated, extended release, oral
- Strength
- 8.5 mg
- Approval
- NDA authorized generic NDA020356
- On the market since
- Feb 27, 2012
- Package NDCs
66993-472-02- Official label
- DailyMed (National Library of Medicine), updated Oct 1, 2021
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