NDC 76420-712
Famotidine 20 mg tablet, film coated
On the label: Asclemed USA, Inc.. It's repackaged: Asclemed USA, Inc. rebottles it from Ascend Laboratories, LLC's NDC 67877-842.
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 |
Repackaging site
- Asclemed USA Inc. dba Enovachem, Torrance, CA, United States · repackages it and relabels it
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
- Jul 8, 2022
- Package NDCs
76420-712-0176420-712-3076420-712-6076420-712-90- Official label
- DailyMed (National Library of Medicine), updated Apr 12, 2024
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