NDC 68071-3786
Famotidine 20 mg tablet, film coated
On the label: NuCare Pharmaceuticals.Inc.. It's repackaged: NuCare Pharmaceuticals.Inc. rebottles it from Camber Pharmaceuticals Inc.'s NDC 31722-017.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Annora Pharma Private Limited | Sangareddy, India | Makes it and tests it | Problems found, fixed voluntarilyMar 28, 2025 · 4 inspections |
Repackaging site
- NuCare Pharmaceuticals,Inc., Orange, CA, United States · repackages it
Product details
- Generic drug
- Famotidine: every company that makes it
- Form
- tablet, film coated, oral
- Strength
- 20 mg
- Approval
- ANDA ANDA215767
- On the market since
- Nov 4, 2021
- Package NDCs
68071-3786-368071-3786-6- Official label
- DailyMed (National Library of Medicine), updated Sep 16, 2026
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?