Pemetrexed
These highlights do not include all the information needed to use PEMETREXED FOR INJECTION safely and effectively. See full prescribing information for PEMETREXED FOR INJECTION. PEMETREXED for injection, for Intravenous Use Initial U.S. Approval: 2004
Approved
Approval ID
0346155f-a455-4044-8d5f-eacb97a8c8f0
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Dec 28, 2023
Manufacturers
FDA
Ingenus Pharmaceuticals, LLC
DUNS: 833250017
Products 2
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
Pemetrexed disodium
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code50742-341
Application NumberANDA204890
Product Classification
M
Marketing Category
C73584
G
Generic Name
Pemetrexed disodium
Product Specifications
Route of AdministrationINTRAVENOUS
Effective DateMay 16, 2022
FDA Product Classification
INGREDIENTS (4)
Sodium hydroxideInactive
Code: 55X04QC32I
Classification: IACT
Hydrochloric acidInactive
Code: QTT17582CB
Classification: IACT
MannitolInactive
Quantity: 500 mg in 20 mL
Code: 3OWL53L36A
Classification: IACT
PEMETREXED DISODIUM HEMIPENTAHYDRATEActive
Quantity: 500 mg in 20 mL
Code: F4GSH45R4C
Classification: ACTIM
Pemetrexed disodium
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code50742-340
Application NumberANDA204890
Product Classification
M
Marketing Category
C73584
G
Generic Name
Pemetrexed disodium
Product Specifications
Route of AdministrationINTRAVENOUS
Effective DateMay 16, 2022
FDA Product Classification
INGREDIENTS (4)
MannitolInactive
Quantity: 106 mg in 4 mL
Code: 3OWL53L36A
Classification: IACT
Sodium hydroxideInactive
Code: 55X04QC32I
Classification: IACT
Hydrochloric acidInactive
Code: QTT17582CB
Classification: IACT
PEMETREXED DISODIUM HEMIPENTAHYDRATEActive
Quantity: 100 mg in 4 mL
Code: F4GSH45R4C
Classification: ACTIM