Selegiline Hydrochloride

Product NDC

0378-9290

11-digit product format

003789290

Labeler code

0378

Product ID

0378-9290_6ed7b687-60bf-43b5-adf3-3090acc992c7

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

selegiline hydrochloride

Dosage form

TABLET

Route

ORAL

Labeler

Mylan Pharmaceuticals Inc.

Application

ANDA074866

Marketing category

ANDA

Marketing start

2010-03-08

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