| NDC Code | 51672-4161-1 |
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| Package Description | 1 BOTTLE in 1 CARTON (51672-4161-1) > 237 mL in 1 BOTTLE |
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| Product NDC | 51672-4161 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Levocetirizine Dihydrochloride |
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| Non-Proprietary Name | Levocetirizine Dihydrochloride |
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| Dosage Form | SOLUTION |
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| Usage | ORAL |
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| Start Marketing Date | 20130726 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA202673 |
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| Manufacturer | Taro Pharmaceuticals U.S.A., inc. |
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| Substance Name | LEVOCETIRIZINE DIHYDROCHLORIDE |
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| Strength | .5 |
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| Strength Unit | mg/mL |
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| Pharmacy Classes | Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC] |
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