Clemastine Fumarate
- Product NDC
- 68151-2456
- 11-digit product format
- 681512456
- Labeler code
- 68151
- Product ID
- 68151-2456_0381b7d6-b261-4c91-9399-bb31be8aa41d
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Clemastine Fumarate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Carilion Materials Management
- Application
- ANDA073458
- Marketing category
- ANDA
- Marketing start
- 1993-10-31
- Marketing end
- 0000-00-00
- Substance
- CLEMASTINE FUMARATE
- Active strength
- 1 mg/1
- NDC exclude flag
- E
- Listing certified through
- 2018-12-31
- 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 |
|---|
| 68151-2456-0 | Clemastine Fumarate | 1 in 1 PACKAGE | TABLET | 1 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 68151-2456 | CLEMASTINE FUMARATE TABLET [CARILION MATERIALS MANAGEMENT] | 2 | Legacy NDC, 1 package rows | 20140708_74f3a9fb-c35e-4720-9538-0a0afe0a773d.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 68151-2456-0 | 68151245600 | 1 in 1 PACKAGE | Historical |