NDC 64980-737
Famotidine 40 mg per 5 mL powder, for suspension
On the label: Rising Pharma Holdings, Inc..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Appco Pharma LLC | Piscataway, NJ, United States | Makes it, tests it and packages 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
- Aug 20, 2026
- Package NDCs
64980-737-50- Official label
- DailyMed (National Library of Medicine), updated Jun 24, 2026
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