NDC 80005-119
Famotidine 40 mg per 5 mL powder, for suspension
On the label: Carnegie Pharmaceuticals, LLC.
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Carnegie Pharmaceuticals, LLC | Delran, NJ, United States | Makes it, tests it, packages it and labels it | No problems foundOct 31, 2025 · 2 inspections |
Product details
- Generic drug
- Famotidine: every company that makes it
- Form
- powder, for suspension, oral
- Strength
- 40 mg per 5 mL
- Approval
- ANDA ANDA217137
- On the market since
- Aug 10, 2023
- Package NDCs
80005-119-16- Official label
- DailyMed (National Library of Medicine), updated May 30, 2025
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