| NDC Code | 21695-820-14 |
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| Package Description | 14 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (21695-820-14) |
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| Product NDC | 21695-820 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Fexofenadine Hydrochloride And Pseudoephedrine Hydrochloride |
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| Non-Proprietary Name | Fexofenadine Hydrochloride And Pseudoephedrine Hydrochloride |
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| Dosage Form | TABLET, FILM COATED, EXTENDED RELEASE |
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| Usage | ORAL |
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| Start Marketing Date | 20091102 |
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| Marketing Category Name | NDA |
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| Application Number | NDA020786 |
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| Manufacturer | Rebel Distributors Corp |
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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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