Product NDC: | 49035-458 |
Proprietary Name: | equate allergy relief |
Non Proprietary Name: | Cetirizine Hydrochloride |
Active Ingredient(s): | 10 mg/1 & nbsp; Cetirizine Hydrochloride |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 49035-458 |
Labeler Name: | Wal-Mart Stores Inc |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | ANDA078336 |
Marketing Category: | ANDA |
Start Marketing Date: | 20080109 |
Package NDC: | 49035-458-95 |
Package Description: | 1 BOTTLE in 1 CARTON (49035-458-95) > 45 TABLET in 1 BOTTLE |
NDC Code | 49035-458-95 |
Proprietary Name | equate allergy relief |
Package Description | 1 BOTTLE in 1 CARTON (49035-458-95) > 45 TABLET in 1 BOTTLE |
Product NDC | 49035-458 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Cetirizine Hydrochloride |
Dosage Form Name | TABLET |
Route Name | ORAL |
Start Marketing Date | 20080109 |
Marketing Category Name | ANDA |
Labeler Name | Wal-Mart Stores Inc |
Substance Name | CETIRIZINE HYDROCHLORIDE |
Strength Number | 10 |
Strength Unit | mg/1 |
Pharmaceutical Classes |