Exelon - 0078-0324-15 - (rivastigmine tartrate)

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Drug Information of Exelon

Product NDC: 0078-0324
Proprietary Name: Exelon
Non Proprietary Name: rivastigmine tartrate
Active Ingredient(s): 3    mg/1 & nbsp;   rivastigmine tartrate
Administration Route(s): ORAL
Dosage Form(s): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of Exelon

Product NDC: 0078-0324
Labeler Name: Novartis Pharmaceuticals Corporation
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020823
Marketing Category: NDA
Start Marketing Date: 20000430

Package Information of Exelon

Package NDC: 0078-0324-15
Package Description: 30 CAPSULE in 1 BLISTER PACK (0078-0324-15)

NDC Information of Exelon

NDC Code 0078-0324-15
Proprietary Name Exelon
Package Description 30 CAPSULE in 1 BLISTER PACK (0078-0324-15)
Product NDC 0078-0324
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name rivastigmine tartrate
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20000430
Marketing Category Name NDA
Labeler Name Novartis Pharmaceuticals Corporation
Substance Name RIVASTIGMINE TARTRATE
Strength Number 3
Strength Unit mg/1
Pharmaceutical Classes Cholinesterase Inhibitor [EPC],Cholinesterase Inhibitors [MoA]

Complete Information of Exelon


General Information