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Ditropan
Ditropan - 50458-805-01 - (oxybutynin chloride)
Drug Information of Ditropan
| Product NDC: | 50458-805 |
| Proprietary Name: | Ditropan |
| Non Proprietary Name: | oxybutynin chloride |
| Active Ingredient(s): | 5 mg/1 & nbsp; oxybutynin chloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, EXTENDED RELEASE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Ditropan
| Product NDC: | 50458-805 |
| Labeler Name: | Janssen Pharmaceuticals, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA020897 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19990626 |
Package Information of Ditropan
| Package NDC: | 50458-805-01 |
| Package Description: | 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (50458-805-01) |
NDC Information of Ditropan
| NDC Code | 50458-805-01 |
| Proprietary Name | Ditropan |
| Package Description | 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (50458-805-01) |
| Product NDC | 50458-805 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | oxybutynin chloride |
| Dosage Form Name | TABLET, EXTENDED RELEASE |
| Route Name | ORAL |
| Start Marketing Date | 19990626 |
| Marketing Category Name | NDA |
| Labeler Name | Janssen Pharmaceuticals, Inc. |
| Substance Name | OXYBUTYNIN CHLORIDE |
| Strength Number | 5 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Cholinergic Muscarinic Antagonist [EPC],Cholinergic Muscarinic Antagonists [MoA] |
