| NDC Code | 43598-892-35 |
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| Package Description | 2 BLISTER PACK in 1 CARTON (43598-892-35) / 5 TABLET, EXTENDED RELEASE in 1 BLISTER PACK |
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| Product NDC | 43598-892 |
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| Product Type Name | HUMAN OTC 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 | 20220517 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA079043 |
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| Manufacturer | Dr.Reddy's Laboratories Inc |
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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 | Adrenergic alpha-Agonists [MoA], Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC], alpha-Adrenergic Agonist [EPC] |
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