ZALTRAP - 0024-5840-01 - (ziv-aflibercept)

Alphabetical Index


Drug Information of ZALTRAP

Product NDC: 0024-5840
Proprietary Name: ZALTRAP
Non Proprietary Name: ziv-aflibercept
Active Ingredient(s): 100    mg/4mL & nbsp;   ziv-aflibercept
Administration Route(s): INTRAVENOUS
Dosage Form(s): SOLUTION, CONCENTRATE
Coding System: National Drug Codes(NDC)

Labeler Information of ZALTRAP

Product NDC: 0024-5840
Labeler Name: sanofi-aventis U.S. LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: BLA125418
Marketing Category: BLA
Start Marketing Date: 20120803

Package Information of ZALTRAP

Package NDC: 0024-5840-01
Package Description: 1 VIAL in 1 CARTON (0024-5840-01) > 4 mL in 1 VIAL

NDC Information of ZALTRAP

NDC Code 0024-5840-01
Proprietary Name ZALTRAP
Package Description 1 VIAL in 1 CARTON (0024-5840-01) > 4 mL in 1 VIAL
Product NDC 0024-5840
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name ziv-aflibercept
Dosage Form Name SOLUTION, CONCENTRATE
Route Name INTRAVENOUS
Start Marketing Date 20120803
Marketing Category Name BLA
Labeler Name sanofi-aventis U.S. LLC
Substance Name ZIV-AFLIBERCEPT
Strength Number 100
Strength Unit mg/4mL
Pharmaceutical Classes

Complete Information of ZALTRAP


General Information