| NDC Code | 70954-912-10 |
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| Package Description | 473 mL in 1 BOTTLE (70954-912-10) |
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| Product NDC | 70954-912 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Hydroxyzine Hydrochloride |
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| Non-Proprietary Name | Hydroxyzine Hydrochloride |
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| Dosage Form | SOLUTION |
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| Usage | ORAL |
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| Start Marketing Date | 20260115 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA219648 |
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| Manufacturer | ANI Pharmaceuticals, Inc. |
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| Substance Name | HYDROXYZINE DIHYDROCHLORIDE |
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| Strength | 10 |
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| Strength Unit | mg/5mL |
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| Pharmacy Classes | Antihistamine [EPC], Histamine Receptor Antagonists [MoA] |
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