FASLODEX - 0310-0720-50 - (Fulvestrant)

Alphabetical Index


Drug Information of FASLODEX

Product NDC: 0310-0720
Proprietary Name: FASLODEX
Non Proprietary Name: Fulvestrant
Active Ingredient(s): 50    mg/mL & nbsp;   Fulvestrant
Administration Route(s): INTRAMUSCULAR
Dosage Form(s): INJECTION
Coding System: National Drug Codes(NDC)

Labeler Information of FASLODEX

Product NDC: 0310-0720
Labeler Name: AstraZeneca Pharmaceuticals LP
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021344
Marketing Category: NDA
Start Marketing Date: 20101101

Package Information of FASLODEX

Package NDC: 0310-0720-50
Package Description: 1 SYRINGE, GLASS in 1 CARTON (0310-0720-50) > 5 mL in 1 SYRINGE, GLASS

NDC Information of FASLODEX

NDC Code 0310-0720-50
Proprietary Name FASLODEX
Package Description 1 SYRINGE, GLASS in 1 CARTON (0310-0720-50) > 5 mL in 1 SYRINGE, GLASS
Product NDC 0310-0720
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Fulvestrant
Dosage Form Name INJECTION
Route Name INTRAMUSCULAR
Start Marketing Date 20101101
Marketing Category Name NDA
Labeler Name AstraZeneca Pharmaceuticals LP
Substance Name FULVESTRANT
Strength Number 50
Strength Unit mg/mL
Pharmaceutical Classes Estrogen Receptor Antagonist [EPC],Estrogen Receptor Antagonists [MoA],Selective Estrogen Receptor Modulators [MoA]

Complete Information of FASLODEX


General Information