Prednisone

Product NDC

48433-321

11-digit product format

484330321

Labeler code

48433

Product ID

48433-321_f7ee9ca2-5123-4230-9666-8eb07a6de8e4

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Prednisone

Dosage form

TABLET

Route

ORAL

Labeler

Safecor Health, LLC

Application

ANDA040362

Marketing category

ANDA

Marketing start

2014-09-30

Marketing end

0000-00-00

Substance

PREDNISONE

Active strength

20 mg/1

Pharmacologic classes

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

NDC exclude flag

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record