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Gemcitabine Hydrochloride - 0591-3563-55 - (Gemcitabine Hydrochloride)

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Drug Information of Gemcitabine Hydrochloride

Product NDC: 0591-3563
Proprietary Name: Gemcitabine Hydrochloride
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 Hydrochloride

Product NDC: 0591-3563
Labeler Name: Watson Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078759
Marketing Category: ANDA
Start Marketing Date: 20110725

Package Information of Gemcitabine Hydrochloride

Package NDC: 0591-3563-55
Package Description: 1 VIAL in 1 CARTON (0591-3563-55) > 25 mL in 1 VIAL

NDC Information of Gemcitabine Hydrochloride

NDC Code 0591-3563-55
Proprietary Name Gemcitabine Hydrochloride
Package Description 1 VIAL in 1 CARTON (0591-3563-55) > 25 mL in 1 VIAL
Product NDC 0591-3563
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 20110725
Marketing Category Name ANDA
Labeler Name Watson Laboratories, 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 Hydrochloride


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