| 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: | 10019-553-02 | 
| Package Description: | 24 POUCH in 1 BOX (10019-553-02) > 1 PATCH in 1 POUCH > 3 d in 1 PATCH | 
| NDC Code | 10019-553-02 | 
| Proprietary Name | Transderm Scop | 
| Package Description | 24 POUCH in 1 BOX (10019-553-02) > 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] |