NDC 67296-1523
Famotidine 20 mg tablet, film coated
On the label: RedPharm Drug. Inc.. It's repackaged: RedPharm Drug. Inc. rebottles it from Ascend Laboratories, LLC's NDC 67877-842.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| VKT Pharma Private Limited | Srikakulam, India | Makes it | Problems found, fixed voluntarilyFeb 7, 2025 · 2 inspections |
Repackaging site
- RedPharm Drug, Eden Prairie, MN, United States · repackages it
Product details
- Generic drug
- Famotidine: every company that makes it
- Form
- tablet, film coated
- Strength
- 20 mg
- Approval
- ANDA ANDA215630
- On the market since
- Jul 8, 2022
- Package NDCs
67296-1523-3- Official label
- DailyMed (National Library of Medicine), updated Aug 15, 2024
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?