| NDC Code | 51672-2121-4 |
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| Package Description | 1 BOTTLE in 1 CARTON (51672-2121-4) > 60 mL in 1 BOTTLE |
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| Product NDC | 51672-2121 |
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| Product Type Name | HUMAN OTC DRUG |
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| Proprietary Name | Childrens Fexofenadine Hydrochloride |
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| Proprietary Name Suffix | Hives |
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| Non-Proprietary Name | Fexofenadine Hydrochloride |
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| Dosage Form | SUSPENSION |
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| Usage | ORAL |
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| Start Marketing Date | 20171109 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA208123 |
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| Manufacturer | Taro Pharmaceuticals U.S.A., Inc. |
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| Substance Name | FEXOFENADINE HYDROCHLORIDE |
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| Strength | 30 |
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| Strength Unit | mg/5mL |
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| Pharmacy Classes | Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC] |
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