NDC 51655-653
Valsartan 80 mg tablet
On the label: Northwind Pharmaceuticals. It's repackaged: Northwind Pharmaceuticals rebottles it from Solco Healthcare U.S., LLC's NDC 43547-368.
Where the pills inside were made
This label doesn't name the factory that makes the drug. Companies don't have to print it on the label. The maker's name is often on the stock bottle your pharmacy used; you can ask the pharmacist. See the plants Solco Healthcare U.S., LLC names for other drugs.
Repackaging site
- Northwind Health Company, LLC, Indianapolis, IN, United States · repackages it
Recalls
- Jul 13, 2018 · Class II · Prinston Pharmaceutical Inc
CGMP Deviations: Carcinogen impurity detected in API used to manufacture drug product.
Lots: All lots within expiry. - Jul 13, 2018 · Class II · Prinston Pharmaceutical Inc
CGMP Deviations: Carcinogen impurity detected in API used to manufacture drug product.
Lots: All lots within expiry. - Jul 13, 2018 · Class II · Prinston Pharmaceutical Inc
CGMP Deviations: Carcinogen impurity detected in API used to manufacture drug product.
Lots: All lots within expiry. - Jul 13, 2018 · Class II · Prinston Pharmaceutical Inc
CGMP Deviations: Carcinogen impurity detected in API used to manufacture drug product.
Lots: All lots within expiry. - Nov 29, 2017 · Class II · Prinston Pharmaceutical Inc
Failed Tablet/Capsule Specifications: confirmed customer complaint of thicker and heavier tablets in bottle.
Lots: Lot #: 343B17025, Exp 03/31/19
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Valsartan: every company that makes it
- Form
- tablet, oral
- Strength
- 80 mg
- Approval
- ANDA ANDA204821
- On the market since
- Aug 15, 2023
- Package NDCs
51655-653-52- Official label
- DailyMed (National Library of Medicine), updated Jan 1, 2026
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