Famotidine
- Product NDC
- 67296-1795
- 11-digit product format
- 672961795
- Labeler code
- 67296
- Product ID
- 67296-1795_d61f51d8-4e88-a161-e053-2a95a90ad14a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Famotidine
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- RedPharm Drug, Inc.
- Application
- ANDA206530
- Marketing category
- ANDA
- Marketing start
- 2019-06-19
- 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
- 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 |
|---|
| 67296-1795-3 | Famotidine | 30 in 1 BOTTLE | TABLET, FILM COATED | 30 | | 6 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 67296-1795 | FAMOTIDINE TABLET, FILM COATED [REDPHARM DRUG, INC.] | 6 | Legacy NDC, 1 package rows | 20240727_b2e94db0-e737-5ef1-e053-2995a90aaee8.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 67296-1795-3 | 67296179503 | 30 TABLET, FILM COATED in 1 BOTTLE (67296-1795-3) | 2019-06-19 | 0000-00-00 | No | No | Current |