Class II · Moderate risk
Atorvastatin Calcium Tablets
Microbial Contamination of Non-Sterile Products: potential of an elevated bioburden with identification of objectionable organisms.
National Drug Code
Is NDC 0378-3950-05 recalled?
Atorvastatin Calcium · 500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-3950-05)
Yes — this exact package was recalled
1 FDA recall names the code 0378-3950-05 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
- atorvastatin calcium
- Strength
- ATORVASTATIN CALCIUM TRIHYDRATE 10 mg/1
- Form
- Tablet, Film Coated · Oral
- Labeler
- Mylan Pharmaceuticals Inc.
- Type
- Human Prescription Drug
- Product code
- 0378-3950
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
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.