Famotidine
- Product NDC
- 69256-002
- 11-digit product format
- 692560002
- Labeler code
- 69256
- Product ID
- 69256-002_a5ae82c1-a463-40bd-a5d4-4dcc4bfede3f
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Famotidine
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- HARRIS TEETER, LLC
- Application
- ANDA206531
- Marketing category
- ANDA
- Marketing start
- 2022-08-03
- Substance
- FAMOTIDINE
- Active strength
- 10 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 | 10 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 5QZO15J2Z8 |
| Rxcui | 199047 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 69256-002-47 | Famotidine | 1 in 1 CARTON | TABLET, FILM COATED | 1 | | 4 |
| 69256-002-47 | Famotidine | 30 in 1 BOTTLE | TABLET, FILM COATED | 30 | | 4 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 69256-002 | FAMOTIDINE TABLET, FILM COATED [HARRIS TEETER, LLC] | 4 | Current NDC, Legacy NDC, 2 package rows | 20250403_e49e087c-ee20-3174-e053-2995a90a1d09.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 |
|---|
| 69256-002-47 | 69256000247 | 1 BOTTLE in 1 CARTON (69256-002-47) / 30 TABLET, FILM COATED in 1 BOTTLE | 1 bottle | 2022-08-03 | 0000-00-00 | No | No | Current |