NDC 80425-0589
Famotidine 20 mg tablet, film coated
On the label: Advanced Rx Pharmacy of Tennessee, LLC. It's repackaged: Advanced Rx Pharmacy of Tennessee, LLC rebottles it from Novadoz Pharmaceuticals LLC's NDC 72205-145.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| MSN Laboratories Private Limited | Rangareddy (District), India | Makes it and tests it | Problems found, fixed voluntarilyJun 25, 2024 · 1 inspection |
Repackaging site
- Advanced Rx Pharmacy of Tennessee, LLC, Nashville, TN, United States · repackages it
Product details
- Generic drug
- Famotidine: every company that makes it
- Form
- tablet, film coated, oral
- Strength
- 20 mg
- Approval
- ANDA ANDA217400
- On the market since
- Jul 10, 2026
- Package NDCs
80425-0589-180425-0589-280425-0589-3- Official label
- DailyMed (National Library of Medicine), updated Jul 10, 2026
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