| Product NDC: | 52544-041 |
| Proprietary Name: | Gelnique |
| Non Proprietary Name: | Oxybutynin |
| Active Ingredient(s): | 28 mg/.92g & nbsp; Oxybutynin |
| Administration Route(s): | TRANSDERMAL |
| Dosage Form(s): | GEL |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 52544-041 |
| Labeler Name: | Watson Pharma, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA202513 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20120402 |
| Package NDC: | 52544-041-54 |
| Package Description: | 1 BOTTLE, PUMP in 1 CARTON (52544-041-54) > 92 g in 1 BOTTLE, PUMP |
| NDC Code | 52544-041-54 |
| Proprietary Name | Gelnique |
| Package Description | 1 BOTTLE, PUMP in 1 CARTON (52544-041-54) > 92 g in 1 BOTTLE, PUMP |
| Product NDC | 52544-041 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Oxybutynin |
| Dosage Form Name | GEL |
| Route Name | TRANSDERMAL |
| Start Marketing Date | 20120402 |
| Marketing Category Name | NDA |
| Labeler Name | Watson Pharma, Inc. |
| Substance Name | OXYBUTYNIN |
| Strength Number | 28 |
| Strength Unit | mg/.92g |
| Pharmaceutical Classes | Cholinergic Muscarinic Antagonist [EPC],Cholinergic Muscarinic Antagonists [MoA] |