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Rivastigmine Tartrate - 55111-353-05 - (Rivastigmine Tartrate)

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Drug Information of Rivastigmine Tartrate

Product NDC: 55111-353
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: 55111-353
Labeler Name: Dr.Reddy's Laboratories Limited
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077130
Marketing Category: ANDA
Start Marketing Date: 20110901

Package Information of Rivastigmine Tartrate

Package NDC: 55111-353-05
Package Description: 500 CAPSULE in 1 BOTTLE (55111-353-05)

NDC Information of Rivastigmine Tartrate

NDC Code 55111-353-05
Proprietary Name Rivastigmine Tartrate
Package Description 500 CAPSULE in 1 BOTTLE (55111-353-05)
Product NDC 55111-353
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Rivastigmine Tartrate
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20110901
Marketing Category Name ANDA
Labeler Name Dr.Reddy's Laboratories 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


General Information