Fosaprepitant
These highlights do not include all the information needed to use FOSAPREPITANT FOR INJECTION safely and effectively. See full prescribing information for FOSAPREPITANT FOR INJECTION. FOSAPREPITANT for injection, for intravenous use Initial U.S. Approval: 2008
Approved
Approval ID
f34c931c-78b9-90c1-3fa5-bb34a227f2ad
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Sep 6, 2019
Manufacturers
FDA
Dr. Reddy's Laboratories Inc.,
DUNS: 802315887
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
Fosaprepitant
PRODUCT DETAILS
NDC Product Code43598-859
Application NumberANDA209965
Marketing CategoryC73584
Route of AdministrationINTRAVENOUS
Effective DateSeptember 6, 2019
Generic NameFosaprepitant
INGREDIENTS (6)
Anhydrous LactoseInactive
Quantity: 375 mg in 5 mL
Code: 3SY5LH9PMK
Classification: IACT
Polysorbate 80Inactive
Quantity: 75 mg in 5 mL
Code: 6OZP39ZG8H
Classification: IACT
Sodium HydroxideInactive
Code: 55X04QC32I
Classification: IACT
Fosaprepitant DimeglumineActive
Quantity: 150 mg in 5 mL
Code: D35FM8T64X
Classification: ACTIR
Edetate SodiumInactive
Quantity: 18.8 mg in 5 mL
Code: MP1J8420LU
Classification: IACT
Hydrochloric AcidInactive
Code: QTT17582CB
Classification: IACT