Prednisone

Product NDC

42708-047

11-digit product format

427080047

Labeler code

42708

Product ID

42708-047_981c7adc-8c9e-49f3-80ff-d934fb31e05a

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Prednisone

Dosage form

TABLET

Route

ORAL

Labeler

QPharma Inc

Application

ANDA080352

Marketing category

ANDA

Marketing start

1972-04-21

Marketing end

0000-00-00

Substance

PREDNISONE

Active strength

5 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