| Product NDC: | 52544-084 |
| Proprietary Name: | GELNIQUE |
| Non Proprietary Name: | oxybutynin chloride |
| Active Ingredient(s): | 100 mg/g & nbsp; oxybutynin chloride |
| Administration Route(s): | TRANSDERMAL |
| Dosage Form(s): | GEL |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 52544-084 |
| Labeler Name: | Watson Pharma, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA022204 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20090515 |
| Package NDC: | 52544-084-30 |
| Package Description: | 30 PACKET in 1 CARTON (52544-084-30) > 1 g in 1 PACKET |
| NDC Code | 52544-084-30 |
| Proprietary Name | GELNIQUE |
| Package Description | 30 PACKET in 1 CARTON (52544-084-30) > 1 g in 1 PACKET |
| Product NDC | 52544-084 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | oxybutynin chloride |
| Dosage Form Name | GEL |
| Route Name | TRANSDERMAL |
| Start Marketing Date | 20090515 |
| Marketing Category Name | NDA |
| Labeler Name | Watson Pharma, Inc. |
| Substance Name | OXYBUTYNIN CHLORIDE |
| Strength Number | 100 |
| Strength Unit | mg/g |
| Pharmaceutical Classes | Cholinergic Muscarinic Antagonist [EPC],Cholinergic Muscarinic Antagonists [MoA] |