| 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 |