"0555-1021-01" National Drug Code (NDC)

NDC Code	0555-1021-01
Package Description	30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (0555-1021-01)
Product NDC	0555-1021
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Galantamine
Non-Proprietary Name	Galantamine
Dosage Form	CAPSULE, EXTENDED RELEASE
Usage	ORAL
Start Marketing Date	20081015
End Marketing Date	20180531
Marketing Category Name	ANDA
Application Number	ANDA078189
Manufacturer	Teva Pharmaceuticals USA, Inc.
Substance Name	GALANTAMINE HYDROBROMIDE
Strength	16
Strength Unit	mg/1
Pharmacy Classes	Cholinesterase Inhibitor [EPC],Cholinesterase Inhibitors [MoA]