| NDC Code | 0088-1090-55 |
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| Package Description | 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (0088-1090-55) |
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| Product NDC | 0088-1090 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Allegra D-12 Hour |
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| Non-Proprietary Name | Fexofenadine Hydrochloride And Pseudoephedrine Hydrochloride |
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| Dosage Form | TABLET, EXTENDED RELEASE |
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| Usage | ORAL |
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| Start Marketing Date | 19971224 |
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| Marketing Category Name | NDA |
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| Application Number | NDA020786 |
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| Manufacturer | sanofi-aventis U.S. LLC |
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| Substance Name | FEXOFENADINE HYDROCHLORIDE; PSEUDOEPHEDRINE HYDROCHLORIDE |
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| Strength | 60; 120 |
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| Strength Unit | mg/1; mg/1 |
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| Pharmacy Classes | Histamine H1 Receptor Antagonists [MoA],Histamine-1 Receptor Antagonist [EPC],Adrenergic alpha-Agonists [MoA],alpha-Adrenergic Agonist [EPC] |
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