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Galantamine - 59762-0010-1 - (Galantamine)

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Drug Information of Galantamine

Product NDC: 59762-0010
Proprietary Name: Galantamine
Non Proprietary Name: Galantamine
Active Ingredient(s): 12    mg/1 & nbsp;   Galantamine
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Galantamine

Product NDC: 59762-0010
Labeler Name: Greenstone LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090957
Marketing Category: ANDA
Start Marketing Date: 20110329

Package Information of Galantamine

Package NDC: 59762-0010-1
Package Description: 60 TABLET, FILM COATED in 1 BOTTLE (59762-0010-1)

NDC Information of Galantamine

NDC Code 59762-0010-1
Proprietary Name Galantamine
Package Description 60 TABLET, FILM COATED in 1 BOTTLE (59762-0010-1)
Product NDC 59762-0010
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Galantamine
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20110329
Marketing Category Name ANDA
Labeler Name Greenstone LLC
Substance Name GALANTAMINE HYDROBROMIDE
Strength Number 12
Strength Unit mg/1
Pharmaceutical Classes Cholinesterase Inhibitor [EPC],Cholinesterase Inhibitors [MoA]

Complete Information of Galantamine


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