NDC 70518-3829
Famotidine 20 mg tablet, film coated
On the label: Remedyrepack Inc.. It's repackaged: Remedyrepack 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 |
Product details
- Generic drug
- Famotidine: every company that makes it
- Form
- tablet, film coated, oral
- Strength
- 20 mg
- Approval
- ANDA ANDA215630
- On the market since
- Aug 15, 2023
- Package NDCs
70518-3829-070518-3829-170518-3829-270518-3829-370518-3829-470518-3829-570518-3829-670518-3829-770518-3829-870518-3829-9- Official label
- DailyMed (National Library of Medicine), updated Jun 9, 2026
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