Product NDC: | 41167-4320 |
Proprietary Name: | Allegra--D 24 Hour Allergy and Congestion |
Non Proprietary Name: | fexofenadine hydrochloride and pseudoephedrine hydrochloride |
Active Ingredient(s): | 180; 240 mg/1; mg/1 & nbsp; fexofenadine hydrochloride and pseudoephedrine hydrochloride |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET, FILM COATED, EXTENDED RELEASE |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 41167-4320 |
Labeler Name: | Chattem, Inc. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | NDA021704 |
Marketing Category: | NDA |
Start Marketing Date: | 20110303 |
Package NDC: | 41167-4320-3 |
Package Description: | 1 BLISTER PACK in 1 CARTON (41167-4320-3) > 5 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK |
NDC Code | 41167-4320-3 |
Proprietary Name | Allegra--D 24 Hour Allergy and Congestion |
Package Description | 1 BLISTER PACK in 1 CARTON (41167-4320-3) > 5 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK |
Product NDC | 41167-4320 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | fexofenadine hydrochloride and pseudoephedrine hydrochloride |
Dosage Form Name | TABLET, FILM COATED, EXTENDED RELEASE |
Route Name | ORAL |
Start Marketing Date | 20110303 |
Marketing Category Name | NDA |
Labeler Name | Chattem, Inc. |
Substance Name | FEXOFENADINE HYDROCHLORIDE; PSEUDOEPHEDRINE HYDROCHLORIDE |
Strength Number | 180; 240 |
Strength Unit | mg/1; mg/1 |
Pharmaceutical Classes |