NDC 67296-2133
Famotidine 20 mg tablet
On the label: RedPharm Drug. Inc.. It's repackaged: RedPharm Drug. Inc. rebottles it from Lifestar Pharma LLC.'s NDC 70756-051.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Mankind Pharma Limited | Sirmaur, India | Makes it, tests it and packages it | Problems found, fixed voluntarilyFeb 25, 2022 · 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, oral
- Strength
- 20 mg
- Approval
- ANDA ANDA075302
- On the market since
- Oct 19, 2023
- Package NDCs
67296-2133-3- Official label
- DailyMed (National Library of Medicine), updated Dec 24, 2025
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