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Galantamine - 0615-7543-39 - (Galantamine)

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Drug Information of Galantamine

Product NDC: 0615-7543
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: 0615-7543
Labeler Name: NCS HealthCare of KY, Inc dba Vangard Labs
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077590
Marketing Category: ANDA
Start Marketing Date: 20090529

Package Information of Galantamine

Package NDC: 0615-7543-39
Package Description: 30 TABLET, FILM COATED in 1 BLISTER PACK (0615-7543-39)

NDC Information of Galantamine

NDC Code 0615-7543-39
Proprietary Name Galantamine
Package Description 30 TABLET, FILM COATED in 1 BLISTER PACK (0615-7543-39)
Product NDC 0615-7543
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Galantamine
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20090529
Marketing Category Name ANDA
Labeler Name NCS HealthCare of KY, Inc dba Vangard Labs
Substance Name GALANTAMINE HYDROBROMIDE
Strength Number 12
Strength Unit mg/1
Pharmaceutical Classes Cholinesterase Inhibitor [EPC],Cholinesterase Inhibitors [MoA]

Complete Information of Galantamine


General Information