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Galantamine Hydrobromide - 47335-836-08 - (Galantamine Hydrobromide)

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Drug Information of Galantamine Hydrobromide

Product NDC: 47335-836
Proprietary Name: Galantamine Hydrobromide
Non Proprietary Name: Galantamine Hydrobromide
Active Ingredient(s): 16    mg/1 & nbsp;   Galantamine Hydrobromide
Administration Route(s): ORAL
Dosage Form(s): CAPSULE, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of Galantamine Hydrobromide

Product NDC: 47335-836
Labeler Name: Sun Pharma Global FZE
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090178
Marketing Category: ANDA
Start Marketing Date: 20110209

Package Information of Galantamine Hydrobromide

Package NDC: 47335-836-08
Package Description: 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (47335-836-08)

NDC Information of Galantamine Hydrobromide

NDC Code 47335-836-08
Proprietary Name Galantamine Hydrobromide
Package Description 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (47335-836-08)
Product NDC 47335-836
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Galantamine Hydrobromide
Dosage Form Name CAPSULE, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20110209
Marketing Category Name ANDA
Labeler Name Sun Pharma Global FZE
Substance Name GALANTAMINE HYDROBROMIDE
Strength Number 16
Strength Unit mg/1
Pharmaceutical Classes Cholinesterase Inhibitor [EPC],Cholinesterase Inhibitors [MoA]

Complete Information of Galantamine Hydrobromide


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