Class II ยท Moderate risk
Valsartan 320 mg tablets
CGMP Deviations: Carcinogen impurity detected in API used to manufacture drug product.
National Drug Code
Is NDC 71335-0567-02 recalled?
Valsartan · 90 TABLET in 1 BOTTLE (71335-0567-2)
Yes — this exact package was recalled
1 FDA recall names the code 71335-0567-02 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
- valsartan
- Strength
- VALSARTAN 80 mg/1
- Form
- Tablet · Oral
- Labeler
- Bryant Ranch Prepack
- Type
- Human Prescription Drug
- Product code
- 71335-0567
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
- 71335-1767 Butalbital, Acetaminophen, Caffeine 1
- 71335-1795 Methocarbamol 1
Free recall alerts
Know the day your medication is recalled
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