NDC 50090-6724-00 - DESLORATADINE
This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.
- Product NDC
- 50090-6724
- Requested NDC
- 50090-6724-00
- Package NDCs from labels
- 50090-6724-0, 50090-6724-00
- Manufacturer
- A-S Medication Solutions
- Effective date
- 2026-04-16
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| DESLORATADINE - A-S Medication Solutions | A-S Medication Solutions | 2026-04-16 | HUMAN PRESCRIPTION DRUG LABEL |
DailyMed Package Descriptions#
| 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 | 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 |
openFDA label cross-check#
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| Desloratadine | DESLORATADINE | Morepen Bio Inc. | 21174c0f-9204-4c75-b6e6-2f9ada5b535d | 2026-08-26 | Warnings, Adverse reactions | 349420 FVF865388R |
| DESLORATADINE | DESLORATADINE | Lupin Pharmaceuticals, Inc. | 2a90b899-7746-43dc-ac8a-e754428eb30c | 2026-06-30 | Warnings, Adverse reactions | ANDA078352 68180-153 349420 4b7fefd7-7d54-400c-a7b4-b3fc4ada2eb1 2a90b899-7746-43dc-ac8a-e754428eb30c FVF865388R |
| DESLORATADINE | DESLORATADINE | Bryant Ranch Prepack | f84c8de3-a7d3-4e8b-bfb6-04259e79450a | 2026-06-01 | Warnings, Adverse reactions | ANDA078352 349420 FVF865388R |
| Desloratadine | DESLORATADINE | Natco Pharma USA LLC | e4db30a5-48e5-4fe3-8793-30b6866f87c1 | 2026-04-23 | Warnings, Adverse reactions | 349420 FVF865388R |
| DESLORATADINE | DESLORATADINE | A-S Medication Solutions | a3b61ab9-ec20-4831-b69a-fcd913fce540 | 2026-04-16 | Warnings, Adverse reactions | ANDA078352 50090-6724-0 50090-6724 50090672400 349420 716f99a4-0ec2-4f33-9f5d-36b372a8d24a a3b61ab9-ec20-4831-b69a-fcd913fce540 FVF865388R |
| DESLORATADINE | DESLORATADINE | A-S Medication Solutions | 69b9635b-c790-4316-a790-67b0f5512b72 | 2026-04-16 | Warnings, Adverse reactions | ANDA078352 349420 FVF865388R |
| CLARINEX-D 12 HOUR | DESLORATADINE AND PSEUDOEPHEDRINE SULFATE | Organon LLC | 1af66b7a-4ab8-40d8-abdd-22d3310228a8 | 2025-11-12 | Warnings, Adverse reactions | FVF865388R |
| Desloratadine | DESLORATADINE | Bryant Ranch Prepack | cf7f838b-4595-4c81-97b9-e1594347e1bd | 2025-11-06 | Warnings, Adverse reactions | 349420 FVF865388R |
| Desloratadine Oral Solution | DESLORATADINE | INA Pharmaceutics, Inc. | 41d5e0d4-6188-847b-e063-6294a90a2e2f | 2025-10-23 | Warnings, Adverse reactions | FVF865388R |
| Desloratadine | DESLORATADINE | Virtus Pharmaceuticals, LLC | 0fe374d0-c14b-4102-b568-eb79165fc7ef | 2025-07-10 | Warnings, Adverse reactions | 349420 FVF865388R |
| Clarinex | DESLORATADINE | Organon LLC | c671342e-69a2-4ca5-abc2-8166ed4240d4 | 2025-05-17 | Warnings, Adverse reactions | 349420 FVF865388R |
| Desloratadine | DESLORATADINE | Dr. Reddy's Laboratories Limited | e5d1f465-e436-b4fd-d351-07a7b2acb440 | 2024-02-28 | Warnings, Adverse reactions | FVF865388R |
| Desloratadine | DESLORATADINE | A-S Medication Solutions | 36307c2b-6b6a-46a9-9fe4-1798fc72e7b8 | 2023-12-12 | Warnings, Adverse reactions | 349420 FVF865388R |
| Desloratadine | DESLORATADINE | Bionpharma Inc. | 4d094001-b85a-47b3-bc67-a46660384ece | 2023-11-27 | Warnings, Adverse reactions | 349420 FVF865388R |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.