Famotidine
- Product NDC
- 50090-7180
- 11-digit product format
- 500907180
- Labeler code
- 50090
- Product ID
- 50090-7180_c87aa6df-b23d-4398-b904-bcf303f22eeb
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Famotidine
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA215767
- Marketing category
- ANDA
- Marketing start
- 2021-11-04
- 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 |
|---|
| 50090-7180-0 | 50090718000 | 90 TABLET, FILM COATED in 1 BOTTLE (50090-7180-0) | 2024-05-30 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Famotidine | A-S Medication Solutions | 2024-06-03 | HUMAN PRESCRIPTION DRUG LABEL | 1 |