Class III · Low risk
Atorvastatin Calcium Tablets
Presence of Foreign Tablets/Capsules: a single tablet of Pravastatin 40 mg found in bottle of Atorvastatin Calcium 40 mg.
National Drug Code
Is NDC 60505-2580-09 recalled?
Atorvastatin Calcium · 90 TABLET, FILM COATED in 1 BOTTLE (60505-2580-9)
Yes — this exact package was recalled
1 FDA recall names the code 60505-2580-09 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 PROPYLENE GLYCOL SOLVATE 40 mg/1
- Form
- Tablet, Film Coated · Oral
- Labeler
- Apotex Corp.
- Type
- Human Prescription Drug
- Product code
- 60505-2580
Recalls naming this package
Class II · Moderate risk
Atorvastatin Calcium 40mg Tablet
CGMP Deviations
Class II · Moderate risk
Atorvastatin Calcium 40 MG Tablet
Presence of Foreign Tablets/Capsules:179 doses of Valacyclovir HCl 500 mg tablets were repacked in unit dose packslabeled as Atorvastatin Calcium
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
- 60505-0589 Brimonidine Tartrate/Timolol Maleate Ophthalmic Solution 3
- 60505-0829 Fluticasone Propionate 3
- 60505-0595 See recall 2
- 60505-0596 See recall 2
- 60505-0773 See recall 2
- 60505-1003 Ketorolac Tromethamine 2
Free recall alerts
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