| NDC Code | 69844-072-03 |
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| Package Description | 1000 TABLET, FILM COATED in 1 BOTTLE (69844-072-03) |
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| Product NDC | 69844-072 |
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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 | 20230822 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA217652 |
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| Manufacturer | Graviti Pharmaceuticals Private Limited |
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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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