Class II ยท Moderate risk
Atorvastatin Calcium Tablets USP 40 mg
Failed dissolution specifications: lower than specifications
National Drug Code
Is NDC 70377-0079-13 recalled?
Atorvastatin Calcium · 1000 TABLET, FILM COATED in 1 BOTTLE (70377-079-13)
Yes — this exact package was recalled
1 FDA recall names the code 70377-0079-13 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 40 mg/1
- Form
- Tablet, Film Coated · Oral
- Labeler
- Biocon Pharma Inc.
- Type
- Human Prescription Drug
- Product code
- 70377-0079
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
- 70377-0027 See recall 1
- 70377-0038 Posaconazole 1
- 70377-0066 Prazosin hydrochloride 1
- 70377-0067 Prazosin hydrochloride 1
- 70377-0068 Prazosin hydrochloride 1
Free recall alerts
Know the day your medication is recalled
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