| NDC Code | 68382-256-05 |
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| Package Description | 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68382-256-05) |
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| Product NDC | 68382-256 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Oxybutynin |
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| Non-Proprietary Name | Oxybutynin |
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| Dosage Form | TABLET, FILM COATED, EXTENDED RELEASE |
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| Usage | ORAL |
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| Start Marketing Date | 20170810 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA202332 |
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| Manufacturer | Zydus Pharmaceuticals USA Inc. |
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| Substance Name | OXYBUTYNIN CHLORIDE |
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| Strength | 10 |
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| Strength Unit | mg/1 |
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| Pharmacy Classes | Cholinergic Muscarinic Antagonist [EPC], Cholinergic Muscarinic Antagonists [MoA] |
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