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Xyzal
Xyzal - 0024-5800-90 - (levocetirizine dihydrochloride)
Drug Information of Xyzal
| Product NDC: | 0024-5800 |
| 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, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Xyzal
| Product NDC: | 0024-5800 |
| Labeler Name: | Sanofi-Aventis U.S. LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA022064 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20070809 |
Package Information of Xyzal
| Package NDC: | 0024-5800-90 |
| Package Description: | 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0024-5800-90) |
NDC Information of Xyzal
| NDC Code | 0024-5800-90 |
| Proprietary Name | Xyzal |
| Package Description | 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0024-5800-90) |
| Product NDC | 0024-5800 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | levocetirizine dihydrochloride |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20070809 |
| Marketing Category Name | NDA |
| Labeler Name | Sanofi-Aventis U.S. LLC |
| Substance Name | LEVOCETIRIZINE DIHYDROCHLORIDE |
| Strength Number | 5 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Histamine H1 Receptor Antagonists [MoA],Histamine-1 Receptor Antagonist [EPC] |
