NDC 80425-0483
Ibuprofen and famotidine 800 mg / 26.6 mg tablet
On the label: Advanced Rx Pharmacy of Tennessee, LLC. It's repackaged: Advanced Rx Pharmacy of Tennessee, LLC rebottles it from ENDO USA, Inc.'s NDC 49884-366.
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 ENDO USA, Inc. names for other drugs.
Repackaging site
- Advanced Rx Pharmacy of Tennessee, LLC, Nashville, TN, United States · repackages it
Product details
- Generic drug
- Famotidine and Ibuprofen: every company that makes it
- Form
- tablet, oral
- Strength
- 800 mg / 26.6 mg
- Approval
- ANDA ANDA203658
- On the market since
- Mar 22, 2024
- Package NDCs
80425-0483-180425-0483-280425-0483-3- Official label
- DailyMed (National Library of Medicine), updated Jan 30, 2025
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