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Allegra D-12 Hour
Allegra D-12 Hour - 0088-1090-49 - (fexofenadine hydrochloride and pseudoephedrine hydrochloride)
Drug Information of Allegra D-12 Hour
| Product NDC: | 0088-1090 |
| Proprietary Name: | Allegra D-12 Hour |
| Non Proprietary Name: | fexofenadine hydrochloride and pseudoephedrine hydrochloride |
| Active Ingredient(s): | 60; 120 mg/1; mg/1 & nbsp; fexofenadine hydrochloride and pseudoephedrine hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, EXTENDED RELEASE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Allegra D-12 Hour
| Product NDC: | 0088-1090 |
| Labeler Name: | sanofi-aventis U.S. LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA020786 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19971224 |
Package Information of Allegra D-12 Hour
| Package NDC: | 0088-1090-49 |
| Package Description: | 100 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (0088-1090-49) |
NDC Information of Allegra D-12 Hour
| NDC Code | 0088-1090-49 |
| Proprietary Name | Allegra D-12 Hour |
| Package Description | 100 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (0088-1090-49) |
| Product NDC | 0088-1090 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | fexofenadine hydrochloride and pseudoephedrine hydrochloride |
| Dosage Form Name | TABLET, EXTENDED RELEASE |
| Route Name | ORAL |
| Start Marketing Date | 19971224 |
| Marketing Category Name | NDA |
| Labeler Name | sanofi-aventis U.S. LLC |
| Substance Name | FEXOFENADINE HYDROCHLORIDE; PSEUDOEPHEDRINE HYDROCHLORIDE |
| Strength Number | 60; 120 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes | Histamine H1 Receptor Antagonists [MoA],Histamine-1 Receptor Antagonist [EPC],Adrenergic alpha-Agonists [MoA],alpha-Adrenergic Agonist [EPC] |
