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"47335-581-40" National Drug Code (NDC)
Amifostine 1 VIAL, SINGLE-USE in 1 CARTON (47335-581-40) > 10 mL in 1 VIAL, SINGLE-USE
(Sun Pharma Global FZE)
NDC Code
47335-581-40
Package Description
1 VIAL, SINGLE-USE in 1 CARTON (47335-581-40) > 10 mL in 1 VIAL, SINGLE-USE
Product NDC
47335-581
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Amifostine
Non-Proprietary Name
Amifostine
Dosage Form
INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Usage
INTRAVENOUS
Start Marketing Date
20080314
Marketing Category Name
ANDA
Application Number
ANDA077126
Manufacturer
Sun Pharma Global FZE
Substance Name
AMIFOSTINE
Strength
50
Strength Unit
mg/mL
Pharmacy Classes
Cytoprotective Agent [EPC],Free Radical Scavenging Activity [MoA]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/47335-581-40