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Allegra Allergy
Allegra Allergy - 41167-4131-2 - (fexofenadine hydrochloride)
Drug Information of Allegra Allergy
| Product NDC: | 41167-4131 |
| Proprietary Name: | Allegra Allergy |
| Non Proprietary Name: | fexofenadine hydrochloride |
| Active Ingredient(s): | 60 mg/1 & nbsp; fexofenadine hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Allegra Allergy
| Product NDC: | 41167-4131 |
| Labeler Name: | Chattem, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | NDA020872 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20110303 |
Package Information of Allegra Allergy
| Package NDC: | 41167-4131-2 |
| Package Description: | 2 BLISTER PACK in 1 CARTON (41167-4131-2) > 6 TABLET, FILM COATED in 1 BLISTER PACK |
NDC Information of Allegra Allergy
| NDC Code | 41167-4131-2 |
| Proprietary Name | Allegra Allergy |
| Package Description | 2 BLISTER PACK in 1 CARTON (41167-4131-2) > 6 TABLET, FILM COATED in 1 BLISTER PACK |
| Product NDC | 41167-4131 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | fexofenadine hydrochloride |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20110303 |
| Marketing Category Name | NDA |
| Labeler Name | Chattem, Inc. |
| Substance Name | FEXOFENADINE HYDROCHLORIDE |
| Strength Number | 60 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
