Famotidine
- Product NDC
- 67296-2186
- 11-digit product format
- 672962186
- Labeler code
- 67296
- Product ID
- 67296-2186_44f3f815-5d8e-4bc6-e063-6394a90aa4d7
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Famotidine
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Redpharm Drug
- Application
- ANDA217400
- Marketing category
- ANDA
- Marketing start
- 2024-08-06
- 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
Additional Listing Data
- Finished product
- Yes
- Brand name base
- Famotidine
- Listing expiration
- 2026-12-31
Active Ingredients
| Ingredient | Strength |
|---|
| FAMOTIDINE | 20 mg/1 |
Harmonized Identifiers
| Field | Values |
|---|
| Unii | 5QZO15J2Z8 |
| Rxcui | 310273 |
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 |
|---|
| 67296-2186-3 | 67296218603 | 30 TABLET, FILM COATED in 1 BOTTLE (67296-2186-3) | 2024-09-18 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Famotidine | Redpharm Drug | 2025-12-02 | HUMAN PRESCRIPTION DRUG LABEL | 1 |