Greenstone Brand Phenelzine Sulfate

Product NDC

24822-119

11-digit product format

248220119

Labeler code

24822

Product ID

24822-119_ba71c3e0-b529-4bd6-e053-2a95a90a3b10

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

PHENELZINE SULFATE

Dosage form

TABLET

Route

ORAL

Labeler

Farmea

Application

NDA011909

Marketing category

NDA AUTHORIZED GENERIC

Marketing start

1961-06-09

Marketing end

0000-00-00

Substance

PHENELZINE SULFATE

Active strength

15 mg/1

Pharmacologic classes

Monoamine Oxidase Inhibitor [EPC],Monoamine Oxidase Inhibitors [MoA]

NDC exclude flag

No

Listing certified through

2022-12-31

Current FDA listing

Historical FDA.report record