ARIMIDEX - 0310-0201-30 - (Anastrozole)

Alphabetical Index


Drug Information of ARIMIDEX

Product NDC: 0310-0201
Proprietary Name: ARIMIDEX
Non Proprietary Name: Anastrozole
Active Ingredient(s): 1    mg/1 & nbsp;   Anastrozole
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of ARIMIDEX

Product NDC: 0310-0201
Labeler Name: AstraZeneca Pharmaceuticals LP
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020541
Marketing Category: NDA
Start Marketing Date: 19960116

Package Information of ARIMIDEX

Package NDC: 0310-0201-30
Package Description: 30 TABLET in 1 BOTTLE, PLASTIC (0310-0201-30)

NDC Information of ARIMIDEX

NDC Code 0310-0201-30
Proprietary Name ARIMIDEX
Package Description 30 TABLET in 1 BOTTLE, PLASTIC (0310-0201-30)
Product NDC 0310-0201
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Anastrozole
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19960116
Marketing Category Name NDA
Labeler Name AstraZeneca Pharmaceuticals LP
Substance Name ANASTROZOLE
Strength Number 1
Strength Unit mg/1
Pharmaceutical Classes Aromatase Inhibitor [EPC],Aromatase Inhibitors [MoA]

Complete Information of ARIMIDEX


General Information