NDC 51655-312
Famotidine 20 mg tablet
On the label: Northwind Pharmaceuticals. It's repackaged: Northwind Pharmaceuticals rebottles it from Carlsbad Technology, Inc.'s NDC 61442-121.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Carlsbad Technology, Inc. | Carlsbad, CA, United States | Makes it | Problems found, fixed voluntarilyJun 30, 2026 · 12 inspections |
| Carlsbad Technology, Inc. | Carlsbad, CA, United States | Labels it | Problems found, fixed voluntarilyJun 30, 2026 · 12 inspections |
Repackaging site
- Northwind Health Company, LLC, Indianapolis, IN, United States · repackages it
Product details
- Generic drug
- Famotidine: every company that makes it
- Form
- tablet, oral
- Strength
- 20 mg
- Approval
- ANDA ANDA075805
- On the market since
- May 21, 2020
- Package NDCs
51655-312-2051655-312-25- Official label
- DailyMed (National Library of Medicine), updated Jan 1, 2026
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