SOLU-MEDROL

Basic Information

Product Name

SOLU-MEDROL

FDA Product Code

51662-1263

NDC Product Code

51662-1263

Application Number

NDA011856

Marketing Category

C73594

Effective Date

January 29, 2024

Territorial Authority

USA

FDA Title

SOLU-MEDROL® 125MG PER VIAL 2mL ACT-O-VIAL®

Labeling Type

HUMAN PRESCRIPTION DRUG LABEL

Version Number

Quantity: 17.4 mg in 2 mL

Code: GR686LBA74

Class Code: IACT

Quantity: 1.6 mg in 2 mL

Code: KH7I04HPUU

Class Code: IACT

Quantity: 125 mg in 2 mL

Code: LEC9GKY20K

Class Code: ACTIM

Code: X4W7ZR7023