Famotidine
- Product NDC
- 50436-1000
- 11-digit product format
- 504361000
- Labeler code
- 50436
- Product ID
- 50436-1000_5d747b2d-0ff7-41f5-933f-2b374b0f581a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Famotidine
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Unit Dose Services
- Application
- ANDA078916
- Marketing category
- ANDA
- Marketing start
- 2016-01-29
- Marketing end
- 0000-00-00
- 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
- 2020-12-31
- 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 |
|---|
| 50436-1000-1 | Famotidine | 30 in 1 BOTTLE | TABLET | 30 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50436-1000 | FAMOTIDINE TABLET [UNIT DOSE SERVICES] | 2 | Legacy NDC, 1 package rows | 20170518_1fa09253-1c3e-4378-bb3e-c732f92c3ae9.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 50436-1000-1 | 50436100001 | 30 in 1 BOTTLE | Historical |