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Gemcitabine Hydrochloride - Gemcitabine Hydrochloride

Navigation: NDC > Supplier starting with: A > APP PHARMACEUTICALS, LLC
Field Value
NDC Code: 63323-102
Proprietary Name: Gemcitabine Hydrochloride
Suffix:
Non-Proprietary Name: Gemcitabine Hydrochloride
Dosage Form: INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Method: INTRAVENOUS
Original Marketing Date: 12-09-2011
Category Name: ANDA
Application Number: ANDA077983
Labeler: APP PHARMACEUTICALS, LLC
Substance Name: GEMCITABINE HYDROCHLORIDE
Active Numerator Strength: 200
Active Ingredient Unit: mg/5mL
Pharm Classes: Nucleic Acid Synthesis Inhibitors [MoA],Nucleoside Metabolic Inhibitor [EPC]
DEA Schedule: