Famotidine
- Product NDC
- 80425-0329
- 11-digit product format
- 804250329
- Labeler code
- 80425
- Product ID
- 80425-0329_2a9c0c91-2b34-4def-e063-6294a90a58ef
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Famotidine
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Advanced Rx Pharmacy of Tennessee, LLC
- Application
- ANDA215767
- Marketing category
- ANDA
- Marketing start
- 2023-04-24
- Substance
- FAMOTIDINE
- Active strength
- 20 mg/1
- Pharmacologic classes
- Histamine H2 Receptor Antagonists [MoA], Histamine-2 Receptor Antagonist [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 5QZO15J2Z8 | FAMOTIDINE | 76824-35-6 | FAMOTIDINE |
Packages
| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 80425-0329-1 | 80425032901 | 30 TABLET, FILM COATED in 1 BOTTLE (80425-0329-1) | 2023-04-24 | No | No | Historical |
| 80425-0329-2 | 80425032902 | 60 TABLET, FILM COATED in 1 BOTTLE (80425-0329-2) | 2023-04-24 | No | No | Historical |
| 80425-0329-3 | 80425032903 | 90 TABLET, FILM COATED in 1 BOTTLE (80425-0329-3) | 2023-04-24 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Famotidine Tablet | Advanced Rx Pharmacy of Tennessee, LLC | 2024-12-31 | HUMAN PRESCRIPTION DRUG LABEL | 2 |