MethylPREDNISolone

Product NDC

68788-9218

11-digit product format

687889218

Labeler code

68788

Product ID

68788-9218_8c5b43dd-4490-42b0-8fa8-33ff8b41d58f

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

methylprednisolone

Dosage form

TABLET

Route

ORAL

Labeler

Preferred Pharmaceuticals, Inc.

Application

ANDA040183

Marketing category

ANDA

Marketing start

2014-10-08

Marketing end

0000-00-00

Substance

METHYLPREDNISOLONE

Active strength

4 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