PredniSONE

Product NDC

0615-1542

11-digit product format

006151542

Labeler code

0615

Product ID

0615-1542_bff5ebfc-cfba-4130-b971-26b98a38e026

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

PredniSONE

Dosage form

TABLET

Route

ORAL

Labeler

NCS HealthCare of KY, Inc dba Vangard Labs

Application

ANDA087342

Marketing category

ANDA

Marketing start

2003-02-13

Marketing end

0000-00-00

Substance

PREDNISONE

Active strength

20 mg/1

Pharmacologic classes

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

NDC exclude flag

E

Listing certified through

2018-12-31

Current FDA listing

Historical FDA.report record