FIRMAGON - 55566-8401-1 - (degarelix)

Alphabetical Index


Drug Information of FIRMAGON

Product NDC: 55566-8401
Proprietary Name: FIRMAGON
Non Proprietary Name: degarelix
Active Ingredient(s): 40    mg/mL & nbsp;   degarelix
Administration Route(s): SUBCUTANEOUS
Dosage Form(s): POWDER, METERED
Coding System: National Drug Codes(NDC)

Labeler Information of FIRMAGON

Product NDC: 55566-8401
Labeler Name: Ferring Pharmaceuticals Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA022201
Marketing Category: NDA
Start Marketing Date: 20090302

Package Information of FIRMAGON

Package NDC: 55566-8401-1
Package Description: 2 VIAL, GLASS in 1 CARTON (55566-8401-1) > 3 mL in 1 VIAL, GLASS (55566-8401-0)

NDC Information of FIRMAGON

NDC Code 55566-8401-1
Proprietary Name FIRMAGON
Package Description 2 VIAL, GLASS in 1 CARTON (55566-8401-1) > 3 mL in 1 VIAL, GLASS (55566-8401-0)
Product NDC 55566-8401
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name degarelix
Dosage Form Name POWDER, METERED
Route Name SUBCUTANEOUS
Start Marketing Date 20090302
Marketing Category Name NDA
Labeler Name Ferring Pharmaceuticals Inc.
Substance Name DEGARELIX ACETATE
Strength Number 40
Strength Unit mg/mL
Pharmaceutical Classes

Complete Information of FIRMAGON


General Information