NDC 69238-2090
Famotidine 40 mg per 5 mL powder, for suspension
On the label: Amneal Pharmaceuticals.
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Amneal Pharmaceuticals of New York, LLC | Brookhaven, NY, United States | Makes it, tests it, packages it and labels it | No problems foundSep 25, 2026 · 14 inspections |
Product details
- Generic drug
- Famotidine: every company that makes it
- Form
- powder, for suspension, oral
- Strength
- 40 mg per 5 mL
- Approval
- ANDA ANDA216427
- On the market since
- Aug 5, 2022
- Package NDCs
69238-2090-4- Official label
- DailyMed (National Library of Medicine), updated Aug 30, 2021
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?