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FINASTERIDE - FINASTERIDE

Navigation: NDC > Supplier starting with: S > SUN PHARMA GLOBAL FZE
Field Value
NDC Code: 47335-715
Proprietary Name: FINASTERIDE
Suffix:
Non-Proprietary Name: FINASTERIDE
Dosage Form: TABLET, FILM COATED
Method: ORAL
Original Marketing Date: 18-08-2011
Category Name: ANDA
Application Number: ANDA090507
Labeler: SUN PHARMA GLOBAL FZE
Substance Name: FINASTERIDE
Active Numerator Strength: 5
Active Ingredient Unit: mg/1
Pharm Classes: 5-alpha Reductase Inhibitor [EPC],5-alpha Reductase Inhibitors [MoA]
DEA Schedule: