Galantamine

Product NDC

63739-708

11-digit product format

637390708

Labeler code

63739

Product ID

63739-708_78dc6257-0511-400c-9ad7-585521e19323

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Galantamine

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

McKesson Corporation dba SKY Packaging

Application

ANDA090957

Marketing category

ANDA

Marketing start

2011-03-29

Marketing end

0000-00-00

Substance

GALANTAMINE HYDROBROMIDE

Active strength

8 mg/1

Pharmacologic classes

Cholinesterase Inhibitor [EPC],Cholinesterase Inhibitors [MoA]

NDC exclude flag

No

Listing certified through

2020-12-31

Current FDA listing

Historical FDA.report record