EMFLAZA

Product NDC

42998-504

11-digit product format

429980504

Labeler code

42998

Product ID

42998-504_4e001bac-ce04-4262-96f4-8b23161f9e55

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

deflazacort

Dosage form

TABLET

Route

ORAL

Labeler

Marathon Pharmaceuticals, LLC

Application

NDA208684

Marketing category

NDA

Marketing start

2017-02-09

Marketing end

2020-06-30

Substance

DEFLAZACORT

Active strength

36 mg/1

Pharmacologic classes

Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record