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] |