Prednisone

Product NDC

55700-733

11-digit product format

557000733

Labeler code

55700

Product ID

55700-733_ce36538e-9097-427f-9d8d-71851e34bf7b

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Prednisone

Dosage form

TABLET

Route

ORAL

Labeler

Quality Care Products, LLC

Application

ANDA040392

Marketing category

ANDA

Marketing start

2019-03-15

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