NDC 70518-4395
Famotidine 20 mg tablet, film coated
On the label: Remedyrepack Inc.. It's repackaged: Remedyrepack 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 |
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 21, 2025
- Package NDCs
70518-4395-070518-4395-170518-4395-2- Official label
- DailyMed (National Library of Medicine), updated Apr 24, 2026
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