Famotidine
- Product NDC
- 71872-7366
- 11-digit product format
- 718727366
- Labeler code
- 71872
- Product ID
- 71872-7366_4e803491-8031-50d0-e063-6294a90a5c8d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Famotidine
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAVENOUS
- Labeler
- Medical Purchasing Solutions, LLC
- Application
- ANDA075622
- Marketing category
- ANDA
- Marketing start
- 2024-12-15
- Substance
- FAMOTIDINE
- Active strength
- 10 mg/mL
- Pharmacologic classes
- Histamine H2 Receptor Antagonists [MoA], Histamine-2 Receptor Antagonist [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Famotidine
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| FAMOTIDINE | 10 mg/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 5QZO15J2Z8 |
| Rxcui | 1743833 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 71872-7366-1 | Famotidine | 1 in 1 BAG | INJECTION, SOLUTION | 1 | | 1 |
| 71872-7366-1 | Famotidine | 2 mL in 1 VIAL | INJECTION, SOLUTION | 2 | | 1 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 71872-7366-1 | 71872736601 | 1 VIAL in 1 BAG (71872-7366-1) / 2 mL in 1 VIAL | 1 vial | 2026-02-20 | No | No | Current |