Product NDC: | 41167-4244 |
Proprietary Name: | Childrens Allegra Allergy |
Non Proprietary Name: | Fexofenadine Hydrochloride |
Active Ingredient(s): | 6 mg/mL & nbsp; Fexofenadine Hydrochloride |
Administration Route(s): | ORAL |
Dosage Form(s): | SUSPENSION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 41167-4244 |
Labeler Name: | Chattem, Inc. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | NDA201373 |
Marketing Category: | NDA |
Start Marketing Date: | 20110303 |
Package NDC: | 41167-4244-4 |
Package Description: | 1 BOTTLE in 1 CARTON (41167-4244-4) > 120 mL in 1 BOTTLE |
NDC Code | 41167-4244-4 |
Proprietary Name | Childrens Allegra Allergy |
Package Description | 1 BOTTLE in 1 CARTON (41167-4244-4) > 120 mL in 1 BOTTLE |
Product NDC | 41167-4244 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Fexofenadine Hydrochloride |
Dosage Form Name | SUSPENSION |
Route Name | ORAL |
Start Marketing Date | 20110303 |
Marketing Category Name | NDA |
Labeler Name | Chattem, Inc. |
Substance Name | FEXOFENADINE HYDROCHLORIDE |
Strength Number | 6 |
Strength Unit | mg/mL |
Pharmaceutical Classes |