NDC 0677-1979
Nisoldipine 17 mg tablet, film coated, extended release
On the label: United Research Laboratories, Inc..
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 United Research Laboratories, Inc. names for other drugs.
Recalls
- Mar 8, 2012 · Class II · Shionogi Inc.
Failed USP Dissolution Test Requirements: Out of Specification dissolution result at 18 month time point
Lots: Lot number: 2021956, Exp; 01/2013
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
- Strength
- 17 mg
- Approval
- NDA authorized generic NDA020356
- On the market since
- Sep 1, 2009
- Package NDCs
0677-1979-01- Official label
- DailyMed (National Library of Medicine), updated Sep 1, 2009
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?