Vinblastine Sulfate
vinBLAStine Sulfate
Approved
Approval ID
f073b58e-56d6-4c8d-a2ce-b37719402d77
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Dec 31, 2019
Manufacturers
FDA
Fresenius Kabi USA, LLC
DUNS: 608775388
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
VINBLASTINE SULFATE
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code63323-278
Application NumberANDA089515
Product Classification
M
Marketing Category
C73584
G
Generic Name
VINBLASTINE SULFATE
Product Specifications
Route of AdministrationINTRAVENOUS
Effective DateDecember 31, 2019
FDA Product Classification
INGREDIENTS (4)
SODIUM CHLORIDEInactive
Quantity: 9 mg in 1 mL
Code: 451W47IQ8X
Classification: IACT
BENZYL ALCOHOLInactive
Code: LKG8494WBH
Classification: IACT
VINBLASTINE SULFATEActive
Quantity: 1 mg in 1 mL
Code: N00W22YO2B
Classification: ACTIB
WATERInactive
Code: 059QF0KO0R
Classification: IACT