| NDC Code | 71309-112-18 |
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| Package Description | 180 TABLET, FILM COATED in 1 BOTTLE (71309-112-18) |
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| Product NDC | 71309-112 |
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| Product Type Name | HUMAN OTC DRUG |
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| Proprietary Name | Levocetirizine Dihydrochloride |
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| Non-Proprietary Name | Levocetirizine Dihydrochloride |
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| Dosage Form | TABLET, FILM COATED |
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| Usage | ORAL |
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| Start Marketing Date | 20221028 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA213513 |
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| Manufacturer | Safrel Pharmaceuticals LLC |
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| Substance Name | LEVOCETIRIZINE DIHYDROCHLORIDE |
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| Strength | 5 |
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| Strength Unit | mg/1 |
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| Pharmacy Classes | Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC] |
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