FAMOTIDINE
- Product NDC
- 61919-236
- 11-digit product format
- 619190236
- Labeler code
- 61919
- Product ID
- 61919-236_e9d0fb30-5b39-eda2-e053-2995a90a2b14
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- FAMOTIDINE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Direct_Rx
- Application
- ANDA078916
- Marketing category
- ANDA
- Marketing start
- 2019-08-08
- Marketing end
- 0000-00-00
- 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
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 61919-236-60 | FAMOTIDINE | 60 in 1 BOTTLE | TABLET | 60 | | 5 |
| 61919-236-90 | FAMOTIDINE | 90 in 1 BOTTLE | TABLET | 90 | | 5 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 61919-236 | FAMOTIDINE TABLET [DIRECT_RX] | 5 | Legacy NDC, 2 package rows | 20230418_8fa0d2d3-79c8-358c-e053-2995a90a9435.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 |
|---|
| 61919-236-30 | 61919023630 | 30 TABLET in 1 BOTTLE (61919-236-30) | 30 tablet | 2017-10-30 | 0000-00-00 | No | No | Current |
| 61919-236-60 | 61919023660 | 60 TABLET in 1 BOTTLE (61919-236-60) | 60 tablet | 2019-08-08 | 0000-00-00 | No | No | Current |
| 61919-236-90 | 61919023690 | 90 TABLET in 1 BOTTLE (61919-236-90) | 90 tablet | 2019-08-08 | 0000-00-00 | No | No | Current |