Memantine hydrochloride

Product NDC

42291-552

11-digit product format

422910552

Labeler code

42291

Product ID

42291-552_687dde8a-716b-f98f-e053-2991aa0ad0f6

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Memantine

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

AvKARE, Inc.

Application

ANDA090041

Marketing category

ANDA

Marketing start

2016-01-11

Marketing end

0000-00-00

Substance

MEMANTINE HYDROCHLORIDE

Active strength

10 mg/1

Pharmacologic classes

NMDA Receptor Antagonists [MoA],N-methyl-D-aspartate Receptor Antagonist [EPC]

NDC exclude flag

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record