Galantamine

Product NDC

51079-852

11-digit product format

510790852

Labeler code

51079

Product ID

51079-852_7c5f5818-0a28-556a-e053-2991aa0a69cc

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

galantamine

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

Mylan Institutional Inc.

Application

ANDA077590

Marketing category

ANDA

Marketing start

2009-11-09

Marketing end

0000-00-00

Substance

GALANTAMINE HYDROBROMIDE

Active strength

4 mg/1

Pharmacologic classes

Cholinesterase Inhibitor [EPC],Cholinesterase Inhibitors [MoA]

NDC exclude flag

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record