Product NDC: | 12634-987 |
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: | 12634-987 |
Labeler Name: | Apotheca Inc. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | ANDA076677 |
Marketing Category: | ANDA |
Start Marketing Date: | 20100101 |
Package NDC: | 12634-987-80 |
Package Description: | 20 TABLET in 1 BOTTLE, PLASTIC (12634-987-80) |
NDC Code | 12634-987-80 |
Proprietary Name | CETIRIZINE HYDROCHLORIDE |
Package Description | 20 TABLET in 1 BOTTLE, PLASTIC (12634-987-80) |
Product NDC | 12634-987 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | CETIRIZINE HYDROCHLORIDE |
Dosage Form Name | TABLET |
Route Name | ORAL |
Start Marketing Date | 20100101 |
Marketing Category Name | ANDA |
Labeler Name | Apotheca Inc. |
Substance Name | CETIRIZINE HYDROCHLORIDE |
Strength Number | 10 |
Strength Unit | mg/1 |
Pharmaceutical Classes |