DESLORATADINE
- Product NDC
- 50090-6724
- 11-digit product format
- 500906724
- Labeler code
- 50090
- Product ID
- 50090-6724_716f99a4-0ec2-4f33-9f5d-36b372a8d24a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- DESLORATADINE
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA078352
- Marketing category
- ANDA
- Marketing start
- 2013-02-25
- Substance
- DESLORATADINE
- Active strength
- 5 mg/1
- Pharmacologic classes
- Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- DESLORATADINE
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| DESLORATADINE | 5 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | FVF865388R |
| Rxcui | 349420 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 50090-6724-0 | DESLORATADINE | 90 in 1 BOTTLE | TABLET, FILM COATED | 90 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-6724 | DESLORATADINE TABLET, FILM COATED [A-S MEDICATION SOLUTIONS] | 1 | Current NDC, 1 package rows | 20231016_a3b61ab9-ec20-4831-b69a-fcd913fce540.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 50090-6724-0 | 50090672400 | 90 TABLET, FILM COATED in 1 BOTTLE (50090-6724-0) | 2023-10-05 | No | No | Historical |