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Galantamine - 60505-2543-8 - (galantamine hydrobromide)

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Drug Information of Galantamine

Product NDC: 60505-2543
Proprietary Name: Galantamine
Non Proprietary Name: galantamine hydrobromide
Active Ingredient(s): 8    mg/1 & nbsp;   galantamine hydrobromide
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Galantamine

Product NDC: 60505-2543
Labeler Name: Apotex Corp.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077781
Marketing Category: ANDA
Start Marketing Date: 20121105

Package Information of Galantamine

Package NDC: 60505-2543-8
Package Description: 1000 TABLET, FILM COATED in 1 BOTTLE (60505-2543-8)

NDC Information of Galantamine

NDC Code 60505-2543-8
Proprietary Name Galantamine
Package Description 1000 TABLET, FILM COATED in 1 BOTTLE (60505-2543-8)
Product NDC 60505-2543
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name galantamine hydrobromide
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20121105
Marketing Category Name ANDA
Labeler Name Apotex Corp.
Substance Name GALANTAMINE HYDROBROMIDE
Strength Number 8
Strength Unit mg/1
Pharmaceutical Classes Cholinesterase Inhibitor [EPC],Cholinesterase Inhibitors [MoA]

Complete Information of Galantamine


General Information