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ALLEGRA
ALLEGRA - 0088-1097-10 - (fexofenadine hydrochloride)
Drug Information of ALLEGRA
| Product NDC: | 0088-1097 |
| Proprietary Name: | ALLEGRA |
| 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) |
Labeler Information of ALLEGRA
| Product NDC: | 0088-1097 |
| Labeler Name: | sanofi-aventis U.S. LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA021963 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20061016 |
Package Information of ALLEGRA
| Package NDC: | 0088-1097-10 |
| Package Description: | 30 mL in 1 BOTTLE (0088-1097-10) |
NDC Information of ALLEGRA
| NDC Code | 0088-1097-10 |
| Proprietary Name | ALLEGRA |
| Package Description | 30 mL in 1 BOTTLE (0088-1097-10) |
| Product NDC | 0088-1097 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | fexofenadine hydrochloride |
| Dosage Form Name | SUSPENSION |
| Route Name | ORAL |
| Start Marketing Date | 20061016 |
| Marketing Category Name | NDA |
| Labeler Name | sanofi-aventis U.S. LLC |
| Substance Name | FEXOFENADINE HYDROCHLORIDE |
| Strength Number | 6 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Histamine H1 Receptor Antagonists [MoA],Histamine-1 Receptor Antagonist [EPC] |
