NDC 51407-640
Capecitabine 500 mg tablet, film coated
On the label: Golden State Medical Supply, Inc.. It's repackaged: Golden State Medical Supply, Inc. rebottles it from Teva Pharmaceuticals USA, Inc.'s NDC 0093-7474.
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 Teva Pharmaceuticals USA, Inc. names for other drugs.
Repackaging site
- Golden State Medical Supply Inc., Camarillo, CA, United States · repackages it and relabels it
Recalls
- Dec 21, 2015 · Class II · Teva North America
Failed Dissolution Specifications: low test results at the 18 month time-point
Lots: Lot # 3A404012V, Exp. 4/2016
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Capecitabine: every company that makes it
- Form
- tablet, film coated, oral
- Strength
- 500 mg
- Approval
- ANDA ANDA091649
- On the market since
- Sep 16, 2013
- Package NDCs
51407-640-12- Official label
- DailyMed (National Library of Medicine), updated Apr 16, 2026
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?