| NDC Code | 62011-0376-1 |
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| Package Description | 2 BLISTER PACK in 1 CARTON (62011-0376-1) > 10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK |
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| Product NDC | 62011-0376 |
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| Product Type Name | HUMAN OTC 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 | 20171030 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA209116 |
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| Manufacturer | McKESSON Corporation |
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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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