MESNEX
These highlights do not include all the information needed to use safely and effectively. See full prescribing information for . Initial U.S. Approval: 1988
Approved
Approval ID
2e8eebc3-ea75-4c57-bfe1-2c5dc2c37806
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Jul 24, 2018
Manufacturers
FDA
Baxter Healthcare Corporation
DUNS: 005083209
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
MESNA
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code0338-1307
Application NumberNDA019884
Product Classification
M
Marketing Category
C73594
G
Generic Name
MESNA
Product Specifications
Route of AdministrationINTRAVENOUS
Effective DateJuly 24, 2018
FDA Product Classification
INGREDIENTS (4)
MESNAActive
Quantity: 100 mg in 1 mL
Code: NR7O1405Q9
Classification: ACTIB
BENZYL ALCOHOLInactive
Quantity: 1.04 mg in 1 mL
Code: LKG8494WBH
Classification: IACT
EDETATE DISODIUMInactive
Quantity: 0.25 mg in 1 mL
Code: 7FLD91C86K
Classification: IACT
SODIUM HYDROXIDEInactive
Code: 55X04QC32I
Classification: IACT