NDC Code | 0615-8565-39 |
Package Description | 30 TABLET in 1 BLISTER PACK (0615-8565-39) |
Product NDC | 0615-8565 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Proprietary Name | Levocetirizine Dihydrochloride |
Non-Proprietary Name | Levocetirizine Dihydrochloride |
Dosage Form | TABLET |
Usage | ORAL |
Start Marketing Date | 20140909 |
Marketing Category Name | ANDA |
Application Number | ANDA203646 |
Manufacturer | NCS HealthCare of KY, LLC dba Vangard Labs |
Substance Name | LEVOCETIRIZINE DIHYDROCHLORIDE |
Strength | 5 |
Strength Unit | mg/1 |
Pharmacy Classes | Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC] |