Famotidine
- Product NDC
- 50090-6790
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Famotidine
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA215767
- Marketing category
- ANDA
- Substance
- FAMOTIDINE
- Current FDA listing
- Yes
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 50090-6790-0 | 30 TABLET, FILM COATED in 1 BOTTLE (50090-6790-0) | 2023-10-31 | | No | Historical |
| 50090-6790-1 | 90 TABLET, FILM COATED in 1 BOTTLE (50090-6790-1) | 2023-10-31 | | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Famotidine | A-S Medication Solutions | 2023-11-02 | HUMAN PRESCRIPTION DRUG LABEL | 1 |