Prednisone

Product NDC

50090-0101

11-digit product format

500900101

Labeler code

50090

Product ID

50090-0101_b5fbbe12-16cd-48c5-977b-7b7a2e79acc3

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Prednisone

Dosage form

TABLET

Route

ORAL

Labeler

A-S Medication Solutions

Application

ANDA083677

Marketing category

ANDA

Marketing start

2009-08-03

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