Famotidine
- Product NDC
- 53943-101
- 11-digit product format
- 539430101
- Labeler code
- 53943
- Product ID
- 53943-101_a9ec4a5f-1e94-74d2-5fa5-7f032c87e11b
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Famotidine
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Discount Drug Mart, Inc
- Application
- ANDA077367
- Marketing category
- ANDA
- Marketing start
- 2021-01-01
- 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 |
|---|
| 53943-101-25 | Famotidine | 1 in 1 CARTON | TABLET | 1 | | 7 |
| 53943-101-25 | Famotidine | 25 in 1 BOTTLE | TABLET | 25 | | 7 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 53943-101 | FAMOTIDINE TABLET [DISCOUNT DRUG MART, INC] | 6 | Current NDC, Legacy NDC, 2 package rows | 20241024_c5d81352-c45b-3ea1-9974-8a096bd05009.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 53943-101-25 | 53943010125 | 1 BOTTLE in 1 CARTON (53943-101-25) / 25 TABLET in 1 BOTTLE | 1 bottle | 2021-01-01 | 0000-00-00 | No | No | Current |