| NDC Code | 54868-5742-1 |
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| Package Description | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (54868-5742-1) |
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| Product NDC | 54868-5742 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Oxybutynin Chloride |
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| Non-Proprietary Name | Oxybutynin Chloride |
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| Dosage Form | TABLET, FILM COATED, EXTENDED RELEASE |
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| Usage | ORAL |
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| Start Marketing Date | 20070108 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA076702 |
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| Manufacturer | Physicians Total Care, Inc. |
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| Substance Name | OXYBUTYNIN CHLORIDE |
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| Strength | 5 |
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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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