NDC 72789-345
Famotidine 40 mg tablet, film coated
On the label: PD-Rx Pharmaceuticals, Inc.. It's repackaged: PD-Rx Pharmaceuticals, Inc. rebottles it from Ascend Laboratories, LLC's NDC 67877-843.
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
- PD-Rx Pharmaceuticals Inc., Oklahoma City, OK, United States · repackages it
Product details
- Generic drug
- Famotidine: every company that makes it
- Form
- tablet, film coated, oral
- Strength
- 40 mg
- Approval
- ANDA ANDA215630
- On the market since
- Jul 8, 2022
- Package NDCs
72789-345-30- Official label
- DailyMed (National Library of Medicine), updated Oct 29, 2026
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