Product NDC: | 65862-450 |
Proprietary Name: | Cetirizine Hydrochloride |
Non Proprietary Name: | Cetirizine Hydrochloride |
Active Ingredient(s): | 1 mg/mL & nbsp; Cetirizine Hydrochloride |
Administration Route(s): | ORAL |
Dosage Form(s): | SYRUP |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 65862-450 |
Labeler Name: | Aurobindo Pharma Limited |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA090751 |
Marketing Category: | ANDA |
Start Marketing Date: | 20091216 |
Package NDC: | 65862-450-12 |
Package Description: | 1 BOTTLE in 1 CARTON (65862-450-12) > 120 mL in 1 BOTTLE |
NDC Code | 65862-450-12 |
Proprietary Name | Cetirizine Hydrochloride |
Package Description | 1 BOTTLE in 1 CARTON (65862-450-12) > 120 mL in 1 BOTTLE |
Product NDC | 65862-450 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Cetirizine Hydrochloride |
Dosage Form Name | SYRUP |
Route Name | ORAL |
Start Marketing Date | 20091216 |
Marketing Category Name | ANDA |
Labeler Name | Aurobindo Pharma Limited |
Substance Name | CETIRIZINE HYDROCHLORIDE |
Strength Number | 1 |
Strength Unit | mg/mL |
Pharmaceutical Classes | Histamine H1 Receptor Antagonists [MoA],Histamine-1 Receptor Antagonist [EPC] |