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gemcitabine - 55111-686-07 - (gemcitabine)

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Drug Information of gemcitabine

Product NDC: 55111-686
Proprietary Name: gemcitabine
Non Proprietary Name: gemcitabine
Active Ingredient(s): 200    mg/5mL & nbsp;   gemcitabine
Administration Route(s): INTRAVENOUS
Dosage Form(s): INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of gemcitabine

Product NDC: 55111-686
Labeler Name: Dr. Reddy's Laboratories Limited
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA091365
Marketing Category: ANDA
Start Marketing Date: 20110725

Package Information of gemcitabine

Package NDC: 55111-686-07
Package Description: 1 VIAL, SINGLE-USE in 1 CARTON (55111-686-07) > 5 mL in 1 VIAL, SINGLE-USE

NDC Information of gemcitabine

NDC Code 55111-686-07
Proprietary Name gemcitabine
Package Description 1 VIAL, SINGLE-USE in 1 CARTON (55111-686-07) > 5 mL in 1 VIAL, SINGLE-USE
Product NDC 55111-686
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name gemcitabine
Dosage Form Name INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 20110725
Marketing Category Name ANDA
Labeler Name Dr. Reddy's Laboratories Limited
Substance Name GEMCITABINE HYDROCHLORIDE
Strength Number 200
Strength Unit mg/5mL
Pharmaceutical Classes Nucleic Acid Synthesis Inhibitors [MoA],Nucleoside Metabolic Inhibitor [EPC]

Complete Information of gemcitabine


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