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Gemcitabine HCl - 0781-3283-79 - (Gemcitabine hydrochloride)

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Drug Information of Gemcitabine HCl

Product NDC: 0781-3283
Proprietary Name: Gemcitabine HCl
Non Proprietary Name: Gemcitabine hydrochloride
Active Ingredient(s): 1    g/25mL & nbsp;   Gemcitabine hydrochloride
Administration Route(s): INTRAVENOUS
Dosage Form(s): INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Gemcitabine HCl

Product NDC: 0781-3283
Labeler Name: Sandoz Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020509
Marketing Category: NDA
Start Marketing Date: 20100827

Package Information of Gemcitabine HCl

Package NDC: 0781-3283-79
Package Description: 25 mL in 1 VIAL (0781-3283-79)

NDC Information of Gemcitabine HCl

NDC Code 0781-3283-79
Proprietary Name Gemcitabine HCl
Package Description 25 mL in 1 VIAL (0781-3283-79)
Product NDC 0781-3283
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Gemcitabine hydrochloride
Dosage Form Name INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 20100827
Marketing Category Name NDA
Labeler Name Sandoz Inc
Substance Name GEMCITABINE HYDROCHLORIDE
Strength Number 1
Strength Unit g/25mL
Pharmaceutical Classes Nucleic Acid Synthesis Inhibitors [MoA],Nucleoside Metabolic Inhibitor [EPC]

Complete Information of Gemcitabine HCl


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