Product NDC: | 10019-553 |
Proprietary Name: | Transderm Scop |
Non Proprietary Name: | Scopalamine |
Active Ingredient(s): | 1 mg/3d & nbsp; Scopalamine |
Administration Route(s): | TRANSDERMAL |
Dosage Form(s): | PATCH, EXTENDED RELEASE |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 10019-553 |
Labeler Name: | Baxter Healthcare Corporation |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA017874 |
Marketing Category: | NDA |
Start Marketing Date: | 20030101 |
Package NDC: | 10019-553-01 |
Package Description: | 10 POUCH in 1 BOX (10019-553-01) > 1 PATCH in 1 POUCH > 3 d in 1 PATCH |
NDC Code | 10019-553-01 |
Proprietary Name | Transderm Scop |
Package Description | 10 POUCH in 1 BOX (10019-553-01) > 1 PATCH in 1 POUCH > 3 d in 1 PATCH |
Product NDC | 10019-553 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Scopalamine |
Dosage Form Name | PATCH, EXTENDED RELEASE |
Route Name | TRANSDERMAL |
Start Marketing Date | 20030101 |
Marketing Category Name | NDA |
Labeler Name | Baxter Healthcare Corporation |
Substance Name | SCOPOLAMINE |
Strength Number | 1 |
Strength Unit | mg/3d |
Pharmaceutical Classes | Anticholinergic [EPC],Cholinergic Antagonists [MoA] |