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galantamine hydrobromide - 10147-0881-6 - (galantamine hydrobromide)

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Drug Information of galantamine hydrobromide

Product NDC: 10147-0881
Proprietary Name: galantamine hydrobromide
Non Proprietary Name: galantamine hydrobromide
Active Ingredient(s): 4    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 hydrobromide

Product NDC: 10147-0881
Labeler Name: Patriot Pharmaceuticals, LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021169
Marketing Category: NDA
Start Marketing Date: 20010228

Package Information of galantamine hydrobromide

Package NDC: 10147-0881-6
Package Description: 60 TABLET, FILM COATED in 1 BOTTLE (10147-0881-6)

NDC Information of galantamine hydrobromide

NDC Code 10147-0881-6
Proprietary Name galantamine hydrobromide
Package Description 60 TABLET, FILM COATED in 1 BOTTLE (10147-0881-6)
Product NDC 10147-0881
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name galantamine hydrobromide
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20010228
Marketing Category Name NDA
Labeler Name Patriot Pharmaceuticals, LLC
Substance Name GALANTAMINE HYDROBROMIDE
Strength Number 4
Strength Unit mg/1
Pharmaceutical Classes Cholinesterase Inhibitor [EPC],Cholinesterase Inhibitors [MoA]

Complete Information of galantamine hydrobromide


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