NDC 76420-713
Famotidine 40 mg tablet, film coated
On the label: Asclemed USA, Inc.. It's repackaged: Asclemed USA, 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
- Asclemed USA Inc. dba Enovachem, Torrance, CA, United States · relabels 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
76420-713-0176420-713-3076420-713-6076420-713-90- Official label
- DailyMed (National Library of Medicine), updated Apr 12, 2024
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