PrednisoLONE

Product NDC

0603-1567

11-digit product format

006031567

Labeler code

0603

Product ID

0603-1567_5aad3237-1f8b-48f7-bac1-9d30c2cccbb3

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Prednisolone

Dosage form

SYRUP

Route

ORAL

Labeler

Par Pharmaceutical

Application

ANDA040775

Marketing category

ANDA

Marketing start

2007-09-21

Marketing end

2019-06-30

Substance

PREDNISOLONE

Active strength

15 mg/5mL

Pharmacologic classes

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

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record