AMIFOSTINE - 62756-581-42 - (AMIFOSTINE)

Alphabetical Index


Drug Information of AMIFOSTINE

Product NDC: 62756-581
Proprietary Name: AMIFOSTINE
Non Proprietary Name: AMIFOSTINE
Active Ingredient(s): 50    mg/mL & nbsp;   AMIFOSTINE
Administration Route(s): INTRAVENOUS
Dosage Form(s): INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of AMIFOSTINE

Product NDC: 62756-581
Labeler Name: Sun Pharmaceutical Industries Limited
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077126
Marketing Category: ANDA
Start Marketing Date: 20080314

Package Information of AMIFOSTINE

Package NDC: 62756-581-42
Package Description: 3 VIAL, SINGLE-USE in 1 CARTON (62756-581-42) > 10 mL in 1 VIAL, SINGLE-USE

NDC Information of AMIFOSTINE

NDC Code 62756-581-42
Proprietary Name AMIFOSTINE
Package Description 3 VIAL, SINGLE-USE in 1 CARTON (62756-581-42) > 10 mL in 1 VIAL, SINGLE-USE
Product NDC 62756-581
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name AMIFOSTINE
Dosage Form Name INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 20080314
Marketing Category Name ANDA
Labeler Name Sun Pharmaceutical Industries Limited
Substance Name AMIFOSTINE
Strength Number 50
Strength Unit mg/mL
Pharmaceutical Classes

Complete Information of AMIFOSTINE


General Information