FDA Drug Application (202031) for GEMCITABINE HYDROCHLORIDE by LUITPOLD PHARMS INC

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Application Number202031
Product Number001
FormINJECTABLE;INJECTION
DosageEQ 200MG BASE/VIAL
Product Market Status Prescription
Therapeutic Equivalence Evaluation Code AP Injectable aqueous solutions and, in certain instances, intravenous non-aqueous solutions
Reference Drug
Drug NameGEMCITABINE HYDROCHLORIDE
Active IngredientGEMCITABINE HYDROCHLORIDE

Active IngredientCount
List of drugs with Active Ingredient GEMCITABINE HYDROCHLORIDE2


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