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Galantamine - 51079-852-03 - (Galantamine)

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Drug Information of Galantamine

Product NDC: 51079-852
Proprietary Name: Galantamine
Non Proprietary Name: Galantamine
Active Ingredient(s): 4    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: 51079-852
Labeler Name: Mylan Institutional Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077590
Marketing Category: ANDA
Start Marketing Date: 20120831

Package Information of Galantamine

Package NDC: 51079-852-03
Package Description: 30 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-852-03) > 1 TABLET, FILM COATED in 1 BLISTER PACK (51079-852-01)

NDC Information of Galantamine

NDC Code 51079-852-03
Proprietary Name Galantamine
Package Description 30 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-852-03) > 1 TABLET, FILM COATED in 1 BLISTER PACK (51079-852-01)
Product NDC 51079-852
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Galantamine
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20120831
Marketing Category Name ANDA
Labeler Name Mylan Institutional Inc.
Substance Name GALANTAMINE HYDROBROMIDE
Strength Number 4
Strength Unit mg/1
Pharmaceutical Classes Cholinesterase Inhibitor [EPC],Cholinesterase Inhibitors [MoA]

Complete Information of Galantamine


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