| 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 |