NDC 0832-6045
Famotidine 40 mg per 5 mL powder, for suspension
On the label: Upsher-Smith Laboratories, Inc..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Appco Pharma LLC | Piscataway, NJ, United States | Makes it, tests it, packages it and labels it | Problems found, fixed voluntarilyMay 14, 2026 · 9 inspections |
Product details
- Generic drug
- Famotidine: every company that makes it
- Form
- powder, for suspension, oral
- Strength
- 40 mg per 5 mL
- Approval
- ANDA ANDA217655
- On the market since
- Jun 16, 2023
- Package NDCs
0832-6045-100832-6045-150832-6045-50- Official label
- DailyMed (National Library of Medicine), updated Nov 8, 2024
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