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Fexofenadine Hydrochloride
Fexofenadine Hydrochloride - 0480-7253-99 - (Fexofenadine Hydrochloride)
Drug Information of Fexofenadine Hydrochloride
| Product NDC: | 0480-7253 |
| Proprietary Name: | Fexofenadine Hydrochloride |
| Non Proprietary Name: | Fexofenadine Hydrochloride |
| Active Ingredient(s): | 180 mg/1 & nbsp; Fexofenadine Hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Fexofenadine Hydrochloride
| Product NDC: | 0480-7253 |
| Labeler Name: | TEVA Pharmaceutical Industries Ltd. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA076447 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20100917 |
Package Information of Fexofenadine Hydrochloride
| Package NDC: | 0480-7253-99 |
| Package Description: | 47600 TABLET, FILM COATED in 1 CONTAINER (0480-7253-99) |
NDC Information of Fexofenadine Hydrochloride
| NDC Code | 0480-7253-99 |
| Proprietary Name | Fexofenadine Hydrochloride |
| Package Description | 47600 TABLET, FILM COATED in 1 CONTAINER (0480-7253-99) |
| Product NDC | 0480-7253 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Fexofenadine Hydrochloride |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20100917 |
| Marketing Category Name | ANDA |
| Labeler Name | TEVA Pharmaceutical Industries Ltd. |
| Substance Name | FEXOFENADINE HYDROCHLORIDE |
| Strength Number | 180 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Histamine H1 Receptor Antagonists [MoA],Histamine-1 Receptor Antagonist [EPC] |
