| NDC Code | 55111-572-05 |
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| Package Description | 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (55111-572-05) |
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| Product NDC | 55111-572 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Fexofenadine Hcl And Pseudoephedrine Hcl |
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| Non-Proprietary Name | Fexofenadine Hcl And Pseudoephedrine Hcl |
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| Dosage Form | TABLET, EXTENDED RELEASE |
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| Usage | ORAL |
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| Start Marketing Date | 20110128 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA079043 |
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| Manufacturer | Dr.Reddy's Laboratories Limited |
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| Substance Name | FEXOFENADINE HYDROCHLORIDE; PSEUDOEPHEDRINE HYDROCHLORIDE |
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| Strength | 180; 240 |
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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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