Famotidine
- Product NDC
- 21130-023
- 11-digit product format
- 211300023
- Labeler code
- 21130
- Product ID
- 21130-023_53be867e-a578-91cd-9f9d-a0bec097a4ae
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Famotidine
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Albertsons Companies
- Application
- ANDA077367
- Marketing category
- ANDA
- Marketing start
- 2021-11-01
- 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 table| Ingredient | Strength |
|---|
| FAMOTIDINE | 20 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 5QZO15J2Z8 |
| Rxcui | 199047, 310273 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 21130-023-25 | Famotidine | 1 in 1 CARTON | TABLET | 1 | | 3 |
| 21130-023-25 | Famotidine | 25 in 1 BOTTLE | TABLET | 25 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 21130-023 | FAMOTIDINE TABLET [ALBERTSONS COMPANIES] | 2 | Current NDC, 2 package rows | 20241024_27314f55-5e31-703c-b98c-ec89bf308472.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 |
|---|
| 21130-023-25 | 21130002325 | 1 BOTTLE in 1 CARTON (21130-023-25) / 25 TABLET in 1 BOTTLE | 1 bottle | 2023-06-16 | No | No | Historical |