| 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: | 41167-4320-7 | 
| Package Description: | 3 BLISTER PACK in 1 CARTON (41167-4320-7) > 5 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK | 
| NDC Code | 41167-4320-7 | 
| Proprietary Name | Allegra--D 24 Hour Allergy and Congestion | 
| Package Description | 3 BLISTER PACK in 1 CARTON (41167-4320-7) > 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 |