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Rivastigmine Tartrate - 62756-146-61 - (Rivastigmine Tartrate)

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Drug Information of Rivastigmine Tartrate

Product NDC: 62756-146
Proprietary Name: Rivastigmine Tartrate
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 Rivastigmine Tartrate

Product NDC: 62756-146
Labeler Name: Sun Pharmaceutical Industries Limited
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077131
Marketing Category: ANDA
Start Marketing Date: 20100701

Package Information of Rivastigmine Tartrate

Package NDC: 62756-146-61
Package Description: 10 BLISTER PACK in 1 BOX, UNIT-DOSE (62756-146-61) > 10 CAPSULE in 1 BLISTER PACK

NDC Information of Rivastigmine Tartrate

NDC Code 62756-146-61
Proprietary Name Rivastigmine Tartrate
Package Description 10 BLISTER PACK in 1 BOX, UNIT-DOSE (62756-146-61) > 10 CAPSULE in 1 BLISTER PACK
Product NDC 62756-146
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Rivastigmine Tartrate
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20100701
Marketing Category Name ANDA
Labeler Name Sun Pharmaceutical Industries Limited
Substance Name RIVASTIGMINE TARTRATE
Strength Number 3
Strength Unit mg/1
Pharmaceutical Classes Cholinesterase Inhibitor [EPC],Cholinesterase Inhibitors [MoA]

Complete Information of Rivastigmine Tartrate


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