| NDC Code | 60687-675-01 |
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| Package Description | 100 BLISTER PACK in 1 CARTON (60687-675-01) > 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-675-11) |
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| Product NDC | 60687-675 |
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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 | 20220820 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA088618 |
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| Manufacturer | American Health Packaging |
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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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