NDC 63187-655
Valsartan 320 mg tablet
On the label: Proficient Rx LP. It's repackaged: Proficient Rx LP rebottles it from Solco Healthcare U.S., LLC's NDC 43547-370.
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
- Proficient Rx LP, Thousand Oaks, CA, United States · repackages it and relabels 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
- 320 mg
- Approval
- ANDA ANDA204821
- On the market since
- Aug 31, 2015
- Package NDCs
63187-655-3063187-655-6063187-655-90- Official label
- DailyMed (National Library of Medicine), updated Jan 1, 2021
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?