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oxybutynin chloride
oxybutynin chloride - 0378-6015-01 - (oxybutynin chloride)
Drug Information of oxybutynin chloride
| Product NDC: | 0378-6015 |
| Proprietary Name: | oxybutynin chloride |
| Non Proprietary Name: | oxybutynin chloride |
| Active Ingredient(s): | 15 mg/1 & nbsp; oxybutynin chloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, EXTENDED RELEASE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of oxybutynin chloride
| Product NDC: | 0378-6015 |
| Labeler Name: | Mylan Pharmaceuticals Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA020897 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20070510 |
Package Information of oxybutynin chloride
| Package NDC: | 0378-6015-01 |
| Package Description: | 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (0378-6015-01) |
NDC Information of oxybutynin chloride
| NDC Code | 0378-6015-01 |
| Proprietary Name | oxybutynin chloride |
| Package Description | 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (0378-6015-01) |
| Product NDC | 0378-6015 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | oxybutynin chloride |
| Dosage Form Name | TABLET, EXTENDED RELEASE |
| Route Name | ORAL |
| Start Marketing Date | 20070510 |
| Marketing Category Name | NDA |
| Labeler Name | Mylan Pharmaceuticals Inc. |
| Substance Name | OXYBUTYNIN CHLORIDE |
| Strength Number | 15 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Cholinergic Muscarinic Antagonist [EPC],Cholinergic Muscarinic Antagonists [MoA] |
