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Galantamine - 68382-178-01 - (Galantamine)

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Drug Information of Galantamine

Product NDC: 68382-178
Proprietary Name: Galantamine
Non Proprietary Name: Galantamine
Active Ingredient(s): 8    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: 68382-178
Labeler Name: Zydus Pharmaceuticals (USA) Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078898
Marketing Category: ANDA
Start Marketing Date: 20111010

Package Information of Galantamine

Package NDC: 68382-178-01
Package Description: 100 TABLET, FILM COATED in 1 BOTTLE (68382-178-01)

NDC Information of Galantamine

NDC Code 68382-178-01
Proprietary Name Galantamine
Package Description 100 TABLET, FILM COATED in 1 BOTTLE (68382-178-01)
Product NDC 68382-178
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Galantamine
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20111010
Marketing Category Name ANDA
Labeler Name Zydus Pharmaceuticals (USA) Inc.
Substance Name GALANTAMINE HYDROBROMIDE
Strength Number 8
Strength Unit mg/1
Pharmaceutical Classes Cholinesterase Inhibitor [EPC],Cholinesterase Inhibitors [MoA]

Complete Information of Galantamine


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