NDC 83008-091
Famotidine 20 mg tablet, film coated
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 Dr.Reddy's Laboratories Ltd.'s NDC 55111-119.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Dr. Reddy's Laboratories Limited | Medchal-Malkajgiri, India | Makes it and tests it | Problems found, fixed voluntarilyOct 27, 2023 · 8 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, film coated, oral
- Strength
- 20 mg
- Approval
- ANDA ANDA075718
- On the market since
- Sep 18, 2024
- Package NDCs
83008-091-30- Official label
- DailyMed (National Library of Medicine), updated Dec 19, 2024
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