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Exelon
Exelon - 21695-357-30 - (rivastigmine)
Drug Information of Exelon
| Product NDC: | 21695-357 |
| Proprietary Name: | Exelon |
| Non Proprietary Name: | rivastigmine |
| Active Ingredient(s): | 4.6 mg/24[USP'U] & nbsp; rivastigmine |
| Administration Route(s): | TRANSDERMAL |
| Dosage Form(s): | PATCH, EXTENDED RELEASE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Exelon
| Product NDC: | 21695-357 |
| Labeler Name: | Rebel Distributors Corp |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA022083 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20091007 |
Package Information of Exelon
| Package NDC: | 21695-357-30 |
| Package Description: | 30 PATCH in 1 CARTON (21695-357-30) > 24 [USP'U] in 1 PATCH |
NDC Information of Exelon
| NDC Code | 21695-357-30 |
| Proprietary Name | Exelon |
| Package Description | 30 PATCH in 1 CARTON (21695-357-30) > 24 [USP'U] in 1 PATCH |
| Product NDC | 21695-357 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | rivastigmine |
| Dosage Form Name | PATCH, EXTENDED RELEASE |
| Route Name | TRANSDERMAL |
| Start Marketing Date | 20091007 |
| Marketing Category Name | NDA |
| Labeler Name | Rebel Distributors Corp |
| Substance Name | RIVASTIGMINE |
| Strength Number | 4.6 |
| Strength Unit | mg/24[USP'U] |
| Pharmaceutical Classes | Cholinesterase Inhibitor [EPC],Cholinesterase Inhibitors [MoA] |
