| NDC Code | 0378-1065-01 |
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| Package Description | 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (0378-1065-01) |
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| Product NDC | 0378-1065 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Guanfacine Hydrochloride |
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| Non-Proprietary Name | Guanfacine |
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| Dosage Form | TABLET, FILM COATED, EXTENDED RELEASE |
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| Usage | ORAL |
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| Start Marketing Date | 20150602 |
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| End Marketing Date | 20191130 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA202578 |
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| Manufacturer | Mylan Pharmaceuticals Inc. |
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| Substance Name | GUANFACINE HYDROCHLORIDE |
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| Strength | 4 |
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| Strength Unit | mg/1 |
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| Pharmacy Classes | Central alpha-2 Adrenergic Agonist [EPC],Adrenergic alpha2-Agonists [MoA] |
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