Class II · Moderate risk
Atorvastatin Calcium Tablets
CGMP Deviations
National Drug Code
Is NDC 51655-0946-52 recalled?
Atorvastatin Calcium · 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-946-52)
Yes — this exact package was recalled
1 FDA recall names the code 51655-0946-52 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.
1 of these recalls is still ongoing.
- Active ingredient
- Atorvastatin Calcium
- Strength
- ATORVASTATIN CALCIUM TRIHYDRATE 10 mg/1
- Form
- Tablet, Film Coated · Oral
- Labeler
- Northwind Health Company, LLC
- Type
- Human Prescription Drug
- Product code
- 51655-0946
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
- 51655-0109 Doxazosin 1
- 51655-0120 Glimepiride 1
- 51655-0307 Sulfamethoxazole and Trimethoprim 1
- 51655-0320 See recall 1
- 51655-0383 Glimepiride 1
- 51655-0460 See recall 1
Free recall alerts
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