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Fexofenadine Hydrochloride
Fexofenadine Hydrochloride - 0904-6311-89 - (Fexofenadine HCl)
Drug Information of Fexofenadine Hydrochloride
| Product NDC: | 0904-6311 |
| Proprietary Name: | Fexofenadine Hydrochloride |
| Non Proprietary Name: | Fexofenadine HCl |
| Active Ingredient(s): | 180 mg/1 & nbsp; Fexofenadine HCl |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Fexofenadine Hydrochloride
| Product NDC: | 0904-6311 |
| Labeler Name: | Major Pharmaceuticals |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | ANDA079112 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20120904 |
Package Information of Fexofenadine Hydrochloride
| Package NDC: | 0904-6311-89 |
| Package Description: | 90 TABLET in 1 BOTTLE, PLASTIC (0904-6311-89) |
NDC Information of Fexofenadine Hydrochloride
| NDC Code | 0904-6311-89 |
| Proprietary Name | Fexofenadine Hydrochloride |
| Package Description | 90 TABLET in 1 BOTTLE, PLASTIC (0904-6311-89) |
| Product NDC | 0904-6311 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Fexofenadine HCl |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20120904 |
| Marketing Category Name | ANDA |
| Labeler Name | Major Pharmaceuticals |
| Substance Name | FEXOFENADINE HYDROCHLORIDE |
| Strength Number | 180 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
