NDC Code | 70934-400-30 |
Package Description | 30 TABLET in 1 BOTTLE, PLASTIC (70934-400-30) |
Product NDC | 70934-400 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Proprietary Name | Levocetirizine Dihydrochloride |
Non-Proprietary Name | Levocetirizine Dihydrochloride |
Dosage Form | TABLET |
Usage | ORAL |
Start Marketing Date | 20190625 |
Marketing Category Name | ANDA |
Application Number | ANDA203646 |
Manufacturer | Denton Pharma, Inc. DBA Northwind Pharmaceuticals |
Substance Name | LEVOCETIRIZINE DIHYDROCHLORIDE |
Strength | 5 |
Strength Unit | mg/1 |
Pharmacy Classes | Histamine H1 Receptor Antagonists [MoA],Histamine-1 Receptor Antagonist [EPC] |