NDC 67296-2186
Famotidine 20 mg tablet, film coated
On the label: RedPharm Drug. Inc.. It's repackaged: RedPharm Drug. Inc. 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
- RedPharm Drug, Eden Prairie, MN, 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
- Aug 6, 2024
- Package NDCs
67296-2186-3- Official label
- DailyMed (National Library of Medicine), updated Dec 2, 2025
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?