| NDC Code | 68788-7854-3 |
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| Package Description | 30 TABLET in 1 BOTTLE (68788-7854-3) |
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| Product NDC | 68788-7854 |
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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 | TABLET |
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| Usage | ORAL |
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| Start Marketing Date | 20210129 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA204279 |
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| Manufacturer | Preferred Pharmaceuticals Incl |
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| Substance Name | HYDROXYZINE DIHYDROCHLORIDE |
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| Strength | 25 |
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| Strength Unit | mg/1 |
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| Pharmacy Classes | Antihistamine [EPC], Histamine Receptor Antagonists [MoA] |
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