| NDC Code | 53002-3900-2 |
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| Package Description | 20 TABLET, FILM COATED in 1 BOTTLE (53002-3900-2) |
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| Product NDC | 53002-3900 |
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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 | 20121009 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA088618 |
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| Manufacturer | RPK Pharmaceuticals, Inc. |
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| Substance Name | HYDROXYZINE HYDROCHLORIDE |
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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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