Medrol
Approved
Approval ID
4c0dd824-b099-47c3-aaf5-f6ddb873b3ee
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Apr 1, 2010
Manufacturers
FDA
Stat Rx USA
DUNS: 786036330
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
Methylprednisole
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code16590-879
Application NumberNDA011153
Product Classification
M
Marketing Category
C73594
G
Generic Name
Methylprednisole
Product Specifications
Route of AdministrationORAL
Effective DateOctober 25, 2009
FDA Product Classification
INGREDIENTS (1)
methylprednisoloneActive
Quantity: 4 mg in 1 1
Code: X4W7ZR7023
Classification: ACTIB