Class II · Moderate risk
Diovan (valsartan)
Failed Dissolution Specifications
National Drug Code
Is NDC 0078-0359-34 recalled?
Diovan · 90 TABLET in 1 BOTTLE (0078-0359-34)
Yes — this exact package was recalled
2 FDA recalls name the code 0078-0359-34 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
- valsartan
- Strength
- VALSARTAN 160 mg/1
- Form
- Tablet · Oral
- Labeler
- Novartis Pharmaceuticals Corporation
- Type
- Human Prescription Drug
- Product code
- 0078-0359
Recalls naming this package
Class II · Moderate risk
Valsartan
Labeling: Label Mixup: VALSARTAN, Tablet, 160 mg may have potentially been mislabeled as one of the following drugs: PROGESTERONE, Capsule, 100 mg, NDC 00032170801, Pedigree: AD46320_1, EXP: 5/15/2014; CapsuleTOPRIL, Tablet, 6.25 mg (1/2 of 12.5 mg), NDC 00143117101, Pedigree: AD46312_4, EXP: 5/16/2014; MYCOPHENOLATE MOFETIL, Tablet, 500 mg, NDC 00004026001, Pedigree: AD49414_4, EXP: 5/17/2014;
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
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