NDC 49999-237
Famotidine 20 mg tablet
On the label: Lake Erie Medical DBA Quality Care Products LLC. It's repackaged: Lake Erie Medical DBA Quality Care Products LLC 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
- Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC, Location not on file · repackages it
Product details
- Generic drug
- Famotidine: every company that makes it
- Form
- tablet
- Strength
- 20 mg
- Approval
- ANDA ANDA075805
- On the market since
- Apr 16, 2001
- Package NDCs
49999-237-3049999-237-60- Official label
- DailyMed (National Library of Medicine), updated Oct 22, 2019
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