PrednisoLONE

Product NDC

68788-7207

11-digit product format

687887207

Labeler code

68788

Product ID

68788-7207_faa39491-7d8f-4a57-8379-21d8f1d9d301

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Prednisolone

Dosage form

SYRUP

Route

ORAL

Labeler

Preferred Pharmaceuticals Inc

Application

ANDA040775

Marketing category

ANDA

Marketing start

2018-07-23

Marketing end

0000-00-00

Substance

PREDNISOLONE

Active strength

15 mg/5mL

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