NDC 50090-6724
Desloratadine 5 mg tablet, film coated
On the label: A-S Medication Solutions. It's repackaged: A-S Medication Solutions rebottles it from Lupin Pharmaceuticals, Inc.'s NDC 68180-153.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Lupin Limited | Salcette, India | Makes it and packages it | Problems found, fixed voluntarilyNov 21, 2025 · 9 inspections, 1 with FDA action |
Repackaging site
- A-S Medication Solutions LLC, Libertyville, IL, United States · repackages it and relabels it
Recalls
- Dec 20, 2023 · Class II · Lupin Pharmaceuticals Inc.
CGMP Deviations: N-Nitroso Desloratadine impurity result exceeded the acceptable intake limit.
Lots: Lot # G201822, exp. date Jan 2024, 100 count G201823, exp. date Jan 2024, 100 count G201824, exp. date Jan 2024, 500 count
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Desloratadine: every company that makes it
- Form
- tablet, film coated, oral
- Strength
- 5 mg
- Approval
- ANDA ANDA078352
- On the market since
- Feb 25, 2013
- Package NDCs
50090-6724-0- Official label
- DailyMed (National Library of Medicine), updated Apr 16, 2026
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