Class II · Moderate risk
Atorvastatin Calcium Tablets
Presence of foreign substance: Foreign matter has been identified as latex glove in one lot of Atorvastatin Calcium Tablets USP 40 mg.
National Drug Code
Is NDC 63304-0829-05 recalled?
Atorvastatin Calcium · 500 TABLET, FILM COATED in 1 BOTTLE (63304-829-05)
Yes — this exact package was recalled
2 FDA recalls name the code 63304-0829-05 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 40 mg/1
- Form
- Tablet, Film Coated · Oral
- Labeler
- Sun Pharmaceutical Industries Inc.
- Type
- Human Prescription Drug
- Product code
- 63304-0829
Recalls naming this package
Class II · Moderate risk
Atorvastatin Calcium Tablets
Presence of Particulate Matter: Certain batches of Atorvastatin tablets 10 mg, 20 mg and 40 mg may contain small glass particulates.
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
- 63304-0827 See recall 3
- 63304-0616 Doxycycline 2
- 63304-0089 Mesalamine 1
- 63304-0175 Mesalamine 1
- 63304-0240 See recall 1
- 63304-0241 See recall 1
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