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Fexofenadine Hydrochloride
Fexofenadine Hydrochloride - 0904-5961-61 - (Fexofenadine Hydrochloride)
Drug Information of Fexofenadine Hydrochloride
| Product NDC: | 0904-5961 |
| Proprietary Name: | Fexofenadine Hydrochloride |
| Non Proprietary Name: | Fexofenadine Hydrochloride |
| Active Ingredient(s): | 30 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: | 0904-5961 |
| Labeler Name: | Major Pharmaceuticals |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA076502 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20090610 |
Package Information of Fexofenadine Hydrochloride
| Package NDC: | 0904-5961-61 |
| Package Description: | 100 TABLET, FILM COATED in 1 BOX, UNIT-DOSE (0904-5961-61) |
NDC Information of Fexofenadine Hydrochloride
| NDC Code | 0904-5961-61 |
| Proprietary Name | Fexofenadine Hydrochloride |
| Package Description | 100 TABLET, FILM COATED in 1 BOX, UNIT-DOSE (0904-5961-61) |
| Product NDC | 0904-5961 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Fexofenadine Hydrochloride |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20090610 |
| Marketing Category Name | ANDA |
| Labeler Name | Major Pharmaceuticals |
| Substance Name | FEXOFENADINE HYDROCHLORIDE |
| Strength Number | 30 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Histamine H1 Receptor Antagonists [MoA],Histamine-1 Receptor Antagonist [EPC] |
