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"47335-581-42" National Drug Code (NDC)

Amifostine 3 VIAL, SINGLE-USE in 1 CARTON (47335-581-42) > 10 mL in 1 VIAL, SINGLE-USE
(Sun Pharma Global FZE)

NDC Code47335-581-42
Package Description3 VIAL, SINGLE-USE in 1 CARTON (47335-581-42) > 10 mL in 1 VIAL, SINGLE-USE
Product NDC47335-581
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameAmifostine
Non-Proprietary NameAmifostine
Dosage FormINJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
UsageINTRAVENOUS
Start Marketing Date20080314
Marketing Category NameANDA
Application NumberANDA077126
ManufacturerSun Pharma Global FZE
Substance NameAMIFOSTINE
Strength50
Strength Unitmg/mL
Pharmacy ClassesCytoprotective Agent [EPC],Free Radical Scavenging Activity [MoA]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/47335-581-42





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