Vandetanib - 0310-7810-30 - (Vandetanib)

Alphabetical Index


Drug Information of Vandetanib

Product NDC: 0310-7810
Proprietary Name: Vandetanib
Non Proprietary Name: Vandetanib
Active Ingredient(s): 100    mg/1 & nbsp;   Vandetanib
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Vandetanib

Product NDC: 0310-7810
Labeler Name: AstraZeneca Pharmaceuticals LP
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA022405
Marketing Category: NDA
Start Marketing Date: 20110421

Package Information of Vandetanib

Package NDC: 0310-7810-30
Package Description: 30 TABLET in 1 BOTTLE, PLASTIC (0310-7810-30)

NDC Information of Vandetanib

NDC Code 0310-7810-30
Proprietary Name Vandetanib
Package Description 30 TABLET in 1 BOTTLE, PLASTIC (0310-7810-30)
Product NDC 0310-7810
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Vandetanib
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20110421
Marketing Category Name NDA
Labeler Name AstraZeneca Pharmaceuticals LP
Substance Name VANDETANIB
Strength Number 100
Strength Unit mg/1
Pharmaceutical Classes Kinase Inhibitor [EPC],Protein Kinase Inhibitors [MoA]

Complete Information of Vandetanib


General Information