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Rivastigmine Tartrate - 0781-2614-60 - (rivastigmine tartrate)

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Drug Information of Rivastigmine Tartrate

Product NDC: 0781-2614
Proprietary Name: Rivastigmine Tartrate
Non Proprietary Name: rivastigmine tartrate
Active Ingredient(s): 1.5    mg/1 & nbsp;   rivastigmine tartrate
Administration Route(s): ORAL
Dosage Form(s): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of Rivastigmine Tartrate

Product NDC: 0781-2614
Labeler Name: Sandoz Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020823
Marketing Category: NDA
Start Marketing Date: 20000430

Package Information of Rivastigmine Tartrate

Package NDC: 0781-2614-60
Package Description: 60 CAPSULE in 1 BOTTLE (0781-2614-60)

NDC Information of Rivastigmine Tartrate

NDC Code 0781-2614-60
Proprietary Name Rivastigmine Tartrate
Package Description 60 CAPSULE in 1 BOTTLE (0781-2614-60)
Product NDC 0781-2614
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 Sandoz Inc
Substance Name RIVASTIGMINE TARTRATE
Strength Number 1.5
Strength Unit mg/1
Pharmaceutical Classes Cholinesterase Inhibitor [EPC],Cholinesterase Inhibitors [MoA]

Complete Information of Rivastigmine Tartrate


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