Carlsbad Technology, Inc.
Carlsbad, CA, United States · makes it
Problems found, fixed voluntarily Last FDA inspection Jun 30, 2026. 12 inspections on record.
NDC 50436-7371
Famotidine 20 mg tablet
On the label: Unit Dose Services.
It's a repackaged product: Unit Dose Services rebottles it from Carlsbad Technology, Inc.'s NDC 61442-121.
Where the pills inside were made
Carlsbad Technology, Inc.
Carlsbad, CA, United States · labels it
Problems found, fixed voluntarily Last FDA inspection Jun 30, 2026. 12 inspections on record.
Repackaging site
- Unit Dose Services, · repackages it
Product details
- Generic drug
- Famotidine: see every company that makes it
- Form
- tablet
- Strength
- 20 mg
- Approval
- ANDA ANDA075805
- On the market since
- Apr 16, 2001
- Package NDCs
50436-7371-150436-7371-250436-7371-3- Official label
- DailyMed (National Library of Medicine), updated Nov 12, 2012
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?