Home > National Drug Code (NDC) > Galantamine

Galantamine - 65841-755-30 - (Galantamine)

Alphabetical Index


Drug Information of Galantamine

Product NDC: 65841-755
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: 65841-755
Labeler Name: Cadila Healthcare Limited
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078898
Marketing Category: ANDA
Start Marketing Date: 20111010

Package Information of Galantamine

Package NDC: 65841-755-30
Package Description: 10 BLISTER PACK in 1 CARTON (65841-755-30) > 10 TABLET, FILM COATED in 1 BLISTER PACK

NDC Information of Galantamine

NDC Code 65841-755-30
Proprietary Name Galantamine
Package Description 10 BLISTER PACK in 1 CARTON (65841-755-30) > 10 TABLET, FILM COATED in 1 BLISTER PACK
Product NDC 65841-755
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 Cadila Healthcare Limited
Substance Name GALANTAMINE HYDROBROMIDE
Strength Number 4
Strength Unit mg/1
Pharmaceutical Classes Cholinesterase Inhibitor [EPC],Cholinesterase Inhibitors [MoA]

Complete Information of Galantamine


General Information