Product NDC: | 54868-5829 |
Proprietary Name: | Xyzal |
Non Proprietary Name: | levocetirizine dihydrochloride |
Active Ingredient(s): | 5 mg/1 & nbsp; levocetirizine dihydrochloride |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 54868-5829 |
Labeler Name: | Physicians Total Care, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA022064 |
Marketing Category: | NDA |
Start Marketing Date: | 20071106 |
Package NDC: | 54868-5829-0 |
Package Description: | 30 TABLET in 1 BOTTLE (54868-5829-0) |
NDC Code | 54868-5829-0 |
Proprietary Name | Xyzal |
Package Description | 30 TABLET in 1 BOTTLE (54868-5829-0) |
Product NDC | 54868-5829 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | levocetirizine dihydrochloride |
Dosage Form Name | TABLET |
Route Name | ORAL |
Start Marketing Date | 20071106 |
Marketing Category Name | NDA |
Labeler Name | Physicians Total Care, Inc. |
Substance Name | LEVOCETIRIZINE DIHYDROCHLORIDE |
Strength Number | 5 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Histamine H1 Receptor Antagonists [MoA],Histamine-1 Receptor Antagonist [EPC] |