NDC Code | 60505-0403-3 |
Package Description | 1 BOTTLE, PLASTIC in 1 CARTON (60505-0403-3) > 148 mL in 1 BOTTLE, PLASTIC |
Product NDC | 60505-0403 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Proprietary Name | Levocetirizine Dihydrochloride |
Non-Proprietary Name | Levocetirizine Dihydrochloride |
Dosage Form | SOLUTION |
Usage | ORAL |
Start Marketing Date | 20171026 |
End Marketing Date | 20210531 |
Marketing Category Name | ANDA |
Application Number | ANDA202915 |
Manufacturer | Apotex Corp. |
Substance Name | LEVOCETIRIZINE DIHYDROCHLORIDE |
Strength | .5 |
Strength Unit | mg/mL |
Pharmacy Classes | Histamine H1 Receptor Antagonists [MoA],Histamine-1 Receptor Antagonist [EPC] |