Methylprednisolone

Basic Information

Product Name

Methylprednisolone

FDA Product Code

72162-1689

Regulatory Information

NDC Product Code

72162-1689

Application Number

ANDA040189

Marketing Category

C73584

Effective Date

December 7, 2017

Territorial Authority

USA

FDA Title

METHYLPREDNISOLONE TABLETS, USP Rx only

Labeling Type

HUMAN PRESCRIPTION DRUG LABEL

Version Number

100

Active Ingredients

SODIUM LAURYL SULFATE

Code: 368GB5141J

Class Code: IACT

STARCH, CORN

Code: O8232NY3SJ

Class Code: IACT

METHYLPREDNISOLONE

Quantity: 4 mg in 1 1

Code: X4W7ZR7023

Class Code: ACTIB

SILICON DIOXIDE

Code: ETJ7Z6XBU4

Class Code: IACT

ANHYDROUS LACTOSE

Code: 3SY5LH9PMK

Class Code: IACT

MAGNESIUM STEARATE

Code: 70097M6I30

Class Code: IACT

MICROCRYSTALLINE CELLULOSE

Code: OP1R32D61U

Class Code: IACT

SODIUM STARCH GLYCOLATE TYPE A POTATO

Code: 5856J3G2A2

Class Code: IACT

Active Moieties

Code: X4W7ZR7023

Methylprednisolone

Basic Information

Regulatory Information

Company Information

Active Ingredients

SODIUM LAURYL SULFATE

STARCH, CORN

SILICON DIOXIDE

ANHYDROUS LACTOSE

MAGNESIUM STEARATE

MICROCRYSTALLINE CELLULOSE

SODIUM STARCH GLYCOLATE TYPE A POTATO

Active Moieties

METHYLPREDNISOLONE