| NDC Code | 0603-3969-32 |
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| Package Description | 1000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0603-3969-32) |
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| Product NDC | 0603-3969 |
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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, FILM COATED |
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| Usage | ORAL |
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| Start Marketing Date | 20050527 |
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| End Marketing Date | 20161231 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA040580 |
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| Manufacturer | Qualitest Pharmaceuticals |
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| Substance Name | HYDROXYZINE HYDROCHLORIDE |
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| Strength | 50 |
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| Strength Unit | mg/1 |
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| Pharmacy Classes | Antihistamine [EPC],Histamine Receptor Antagonists [MoA] |
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