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AMIFOSTINE - AMIFOSTINE

Navigation: NDC > Supplier starting with: S > SUN PHARMA GLOBAL FZE
Field Value
NDC Code: 47335-581
Proprietary Name: AMIFOSTINE
Suffix:
Non-Proprietary Name: AMIFOSTINE
Dosage Form: INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Method: INTRAVENOUS
Original Marketing Date: 14-03-2008
Category Name: ANDA
Application Number: ANDA077126
Labeler: SUN PHARMA GLOBAL FZE
Substance Name: AMIFOSTINE
Active Numerator Strength: 50
Active Ingredient Unit: mg/mL
Pharm Classes:
DEA Schedule: