NDC 70934-235
Levocetirizine Dihydrochloride 5 mg tablet, film coated
On the label: Denton Pharma, Inc. DBA Northwind Pharmaceuticals.. It's repackaged: Denton Pharma, Inc. DBA Northwind Pharmaceuticals. rebottles it from Macleods Pharmaceuticals Limited's NDC 33342-200.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Macleods Pharmaceuticals Limited | District Solan, India | Makes it, tests it, packages it and labels it | Problems found, fixed voluntarilyOct 20, 2023 · 6 inspections, 2 with FDA action |
Repackaging site
- Denton Pharma, Inc. DBA Northwind Pharmaceuticals, Location not on file · repackages it
Product details
- Generic drug
- Levocetirizine: every company that makes it
- Form
- tablet, film coated
- Strength
- 5 mg
- Approval
- ANDA ANDA205564
- On the market since
- Jan 15, 2019
- Package NDCs
70934-235-30- Official label
- DailyMed (National Library of Medicine), updated Dec 31, 2020
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