Product NDC: | 42254-138 |
Proprietary Name: | Cetirizine hydrochloride |
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: | 42254-138 |
Labeler Name: | Rebel Distributors Corp |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | ANDA077498 |
Marketing Category: | ANDA |
Start Marketing Date: | 20071227 |
Package NDC: | 42254-138-14 |
Package Description: | 14 TABLET in 1 BLISTER PACK (42254-138-14) |
NDC Code | 42254-138-14 |
Proprietary Name | Cetirizine hydrochloride |
Package Description | 14 TABLET in 1 BLISTER PACK (42254-138-14) |
Product NDC | 42254-138 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Cetirizine hydrochloride |
Dosage Form Name | TABLET |
Route Name | ORAL |
Start Marketing Date | 20071227 |
Marketing Category Name | ANDA |
Labeler Name | Rebel Distributors Corp |
Substance Name | CETIRIZINE HYDROCHLORIDE |
Strength Number | 10 |
Strength Unit | mg/1 |
Pharmaceutical Classes |