Class III · Low risk
Pitavastatin Tablets
Presence of foreign tablets/capsules: one Pitavastatin tablet 1mg found in bottle of Pitavastatin tablets 2mg
National Drug Code
Is NDC 72603-0479-01 recalled?
pitavastatin calcium · 90 TABLET, FILM COATED in 1 BOTTLE (72603-479-01)
Yes — this exact package was recalled
1 FDA recall names the code 72603-0479-01 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
- pitavastatin calcium
- Strength
- PITAVASTATIN CALCIUM 2.09 mg/1
- Form
- Tablet, Film Coated · Oral
- Labeler
- NorthStar RxLLC
- Type
- Human Prescription Drug
- Product code
- 72603-0479
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
- 72603-0200 Doxorubicin Hydrochloride 1
Free recall alerts
Know the day your medication is recalled
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