NDC 68071-3584
Famotidine 40 mg tablet, film coated
On the label: NuCare Pharmaceuticals.Inc.. It's repackaged: NuCare Pharmaceuticals.Inc. rebottles it from Ascend Laboratories, LLC's NDC 67877-889.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| VKT Pharma Private Limited | Srikakulam, India | Makes it, tests it, packages it and labels it | Problems found, fixed voluntarilyFeb 7, 2025 · 2 inspections |
Repackaging site
- NuCare Pharmaceuticals,Inc., Orange, CA, 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
- Aug 23, 2023
- Package NDCs
68071-3584-3- Official label
- DailyMed (National Library of Medicine), updated Mar 7, 2024
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