Class III ยท Low risk
Nisoldipine Extended Release Tablets
Failed Dissolution Specifications
National Drug Code
Is NDC 66993-0473-02 recalled?
Nisoldipine · 1 BOTTLE in 1 CARTON (66993-473-02) / 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE
Yes — this exact package was recalled
1 FDA recall names the code 66993-0473-02 directly. A recall still applies to particular lot numbers — compare the lot on your package with the FDA notice below, and talk to your pharmacist before stopping a prescribed medication.
- Active ingredient
- Nisoldipine
- Strength
- NISOLDIPINE 17 mg/1
- Form
- Tablet, Film Coated, Extended Release · Oral
- Labeler
- Prasco Laboratories
- Type
- Human Prescription Drug
- Product code
- 66993-0473
Recalls naming this package
Where to find this code. The NDC is printed on the pharmacy label and on the manufacturer's carton, usually as three groups of digits after “NDC”. The last group is the package size — two bottles of the same medicine can differ only in that group, and a recall may cover one but not the other.
Other recalled products from this labeler
- 66993-0070 See recall 2
- 66993-0019 Albuterol Sulfate HFA 1
- 66993-0408 See recall 1
- 66993-0463 See recall 1
- 66993-0485 See recall 1
- 66993-0680 See recall 1
Free recall alerts
Know the day your medication is recalled
Tell us what you take. When FDA posts a recall announcement or classifies a recall for one of your medications, we email you in plain English, with what to check. No account needed.