Selegiline Hydrochloride

Product NDC

51862-146

11-digit product format

518620146

Labeler code

51862

Product ID

51862-146_285f771f-9083-4b67-b672-8e5748dddc6c

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Selegiline Hydrochloride

Dosage form

TABLET

Route

ORAL

Labeler

Mayne Pharma

Application

ANDA074912

Marketing category

ANDA

Marketing start

2014-05-24

Marketing end

2019-07-31

Substance

SELEGILINE HYDROCHLORIDE

Active strength

5 mg/1

Pharmacologic classes

Monoamine Oxidase Inhibitor [EPC],Monoamine Oxidase Inhibitors [MoA],Monoamine Oxidase Type B Inhibitor [EPC],Monoamine Oxidase-B Inhibitors [MoA]

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record