Class III ยท Low risk
Valsartan Tablets USP
Incorrect/Undeclared Excipient: There is a potential an incorrect grade of excipient was used during manufacturing.
National Drug Code
Is NDC 59746-0361-90 recalled?
valsartan · 90 TABLET in 1 BOTTLE (59746-361-90)
Yes — this exact package was recalled
1 FDA recall names the code 59746-0361-90 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
- Jubilant Cadista Pharmaceuticals Inc.
- Type
- Human Prescription Drug
- Product code
- 59746-0361
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
- 59746-0001 See recall 5
- 59746-0284 Pantoprazole Sodium 5
- 59746-0122 Meclizine Hydrochloride 2
- 59746-0360 valsartan 2
- 59746-0363 See recall 2
- 59746-0003 See recall 1
Free recall alerts
Know the day your medication is recalled
Tell us what you take. When FDA posts a recall announcement or classifies a recall for one of your medications, we email you in plain English, with what to check. No account needed.