NDC Code | 69117-1000-1 |
Package Description | 90 TABLET in 1 BOTTLE (69117-1000-1) |
Product NDC | 69117-1000 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Proprietary Name | Levocetirizine Dihydrochloride |
Non-Proprietary Name | Levocetirizine Dihydrochloride |
Dosage Form | TABLET |
Usage | ORAL |
Start Marketing Date | 20170329 |
Marketing Category Name | ANDA |
Application Number | ANDA203646 |
Manufacturer | YILING PHARMACEUTICAL, INC. |
Substance Name | LEVOCETIRIZINE DIHYDROCHLORIDE |
Strength | 5 |
Strength Unit | mg/1 |
Pharmacy Classes | Histamine H1 Receptor Antagonists [MoA],Histamine-1 Receptor Antagonist [EPC] |