Product NDC: | 53187-189 |
Proprietary Name: | 24 Hour Allergy |
Non Proprietary Name: | Fexofenadine HCl |
Active Ingredient(s): | 180 mg/1 & nbsp; Fexofenadine HCl |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 53187-189 |
Labeler Name: | LIVE BETTER (The Great Atlantic & Pacific Tea Company) |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | ANDA079112 |
Marketing Category: | ANDA |
Start Marketing Date: | 20130320 |
Package NDC: | 53187-189-30 |
Package Description: | 1 BOTTLE in 1 BOX (53187-189-30) > 30 TABLET in 1 BOTTLE |
NDC Code | 53187-189-30 |
Proprietary Name | 24 Hour Allergy |
Package Description | 1 BOTTLE in 1 BOX (53187-189-30) > 30 TABLET in 1 BOTTLE |
Product NDC | 53187-189 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Fexofenadine HCl |
Dosage Form Name | TABLET |
Route Name | ORAL |
Start Marketing Date | 20130320 |
Marketing Category Name | ANDA |
Labeler Name | LIVE BETTER (The Great Atlantic & Pacific Tea Company) |
Substance Name | FEXOFENADINE HYDROCHLORIDE |
Strength Number | 180 |
Strength Unit | mg/1 |
Pharmaceutical Classes |