Product NDC: | 54868-6171 |
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: | 54868-6171 |
Labeler Name: | Physicians Total Care, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA022204 |
Marketing Category: | NDA |
Start Marketing Date: | 20100915 |
Package NDC: | 54868-6171-0 |
Package Description: | 30 PACKET in 1 CARTON (54868-6171-0) > 1 g in 1 PACKET |
NDC Code | 54868-6171-0 |
Proprietary Name | GELNIQUE |
Package Description | 30 PACKET in 1 CARTON (54868-6171-0) > 1 g in 1 PACKET |
Product NDC | 54868-6171 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | oxybutynin chloride |
Dosage Form Name | GEL |
Route Name | TRANSDERMAL |
Start Marketing Date | 20100915 |
Marketing Category Name | NDA |
Labeler Name | Physicians Total Care, Inc. |
Substance Name | OXYBUTYNIN CHLORIDE |
Strength Number | 100 |
Strength Unit | mg/g |
Pharmaceutical Classes | Cholinergic Muscarinic Antagonist [EPC],Cholinergic Muscarinic Antagonists [MoA] |