Famotidine
- Product NDC
- 72162-1737
- 11-digit product format
- 721621737
- Labeler code
- 72162
- Product ID
- 72162-1737_67a6e7f3-04d6-426c-b952-7677a84ace4d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Famotidine
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA075805
- Marketing category
- ANDA
- Marketing start
- 2001-04-16
- Substance
- FAMOTIDINE
- Active strength
- 40 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 table| Ingredient | Strength |
|---|
| FAMOTIDINE | 40 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 5QZO15J2Z8 |
| Rxcui | 284245 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 72162-1737-0 | Famotidine | 1000 in 1 BOTTLE | TABLET | 1000 | | 101 |
| 72162-1737-1 | Famotidine | 100 in 1 BOTTLE | TABLET | 100 | | 101 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 72162-1737 | FAMOTIDINE TABLET [BRYANT RANCH PREPACK] | 101 | Current NDC, 2 package rows | 20240919_67a6e7f3-04d6-426c-b952-7677a84ace4d.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 72162-1737-0 | 72162173700 | 1000 TABLET in 1 BOTTLE (72162-1737-0) | 1000 tablet | 2024-09-17 | No | No | Historical |
| 72162-1737-1 | 72162173701 | 100 TABLET in 1 BOTTLE (72162-1737-1) | 100 tablet | 2024-09-17 | No | No | Historical |