| NDC Code | 68462-361-01 |
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| Package Description | 100 TABLET, FILM COATED in 1 BOTTLE (68462-361-01) |
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| Product NDC | 68462-361 |
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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 | 20080301 |
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| End Marketing Date | 20160901 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA040812 |
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| Manufacturer | Glenmark Generics Inc., USA |
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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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