Prednisone

Product NDC

42708-046

11-digit product format

427080046

Labeler code

42708

Product ID

42708-046_ecc446a6-cb60-4379-aea2-f1c53b9d25ba

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Prednisone

Dosage form

TABLET

Route

ORAL

Labeler

QPharma Inc

Application

ANDA040392

Marketing category

ANDA

Marketing start

2003-02-12

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

2020-12-31

Current FDA listing

Historical FDA.report record