FAMOTIDINE
- Product NDC
- 50090-7829
- 11-digit product format
- 500907829
- Labeler code
- 50090
- Product ID
- 50090-7829_97c3d668-9ecc-4160-b317-d7b4c34de261
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- FAMOTIDINE
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA215630
- Marketing category
- ANDA
- Marketing start
- 2022-07-08
- 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 |
|---|
| 50090-7829-0 | 50090782900 | 90 TABLET, FILM COATED in 1 BOTTLE (50090-7829-0) | 2025-12-17 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| FAMOTIDINE | A-S Medication Solutions | 2025-12-30 | Human Prescription Drug Label | 1 |