Product NDC: | 59726-189 |
Proprietary Name: | Allergy Relief |
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: | 59726-189 |
Labeler Name: | P and L Development of New York Corporation |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | ANDA079112 |
Marketing Category: | ANDA |
Start Marketing Date: | 20130328 |
Package NDC: | 59726-189-05 |
Package Description: | 1 BLISTER PACK in 1 CARTON (59726-189-05) > 5 TABLET in 1 BLISTER PACK |
NDC Code | 59726-189-05 |
Proprietary Name | Allergy Relief |
Package Description | 1 BLISTER PACK in 1 CARTON (59726-189-05) > 5 TABLET in 1 BLISTER PACK |
Product NDC | 59726-189 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Fexofenadine HCl |
Dosage Form Name | TABLET |
Route Name | ORAL |
Start Marketing Date | 20130328 |
Marketing Category Name | ANDA |
Labeler Name | P and L Development of New York Corporation |
Substance Name | FEXOFENADINE HYDROCHLORIDE |
Strength Number | 180 |
Strength Unit | mg/1 |
Pharmaceutical Classes |