| NDC Code | 31722-659-31 |
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| Package Description | 1 BOTTLE in 1 CARTON (31722-659-31) > 148 mL in 1 BOTTLE |
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| Product NDC | 31722-659 |
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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 | 20190401 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA210914 |
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| Manufacturer | Camber Pharmaceuticals, Inc. |
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| Substance Name | LEVOCETIRIZINE DIHYDROCHLORIDE |
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| Strength | 2.5 |
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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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