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Fluorouracil - 10139-063-11 - (Fluorouracil)

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Drug Information of Fluorouracil

Product NDC: 10139-063
Proprietary Name: Fluorouracil
Non Proprietary Name: Fluorouracil
Active Ingredient(s): 50    mg/mL & nbsp;   Fluorouracil
Administration Route(s): INTRAVENOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Fluorouracil

Product NDC: 10139-063
Labeler Name: GeneraMedix
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040743
Marketing Category: ANDA
Start Marketing Date: 20120830

Package Information of Fluorouracil

Package NDC: 10139-063-11
Package Description: 10 VIAL, SINGLE-DOSE in 1 CARTON (10139-063-11) > 10 mL in 1 VIAL, SINGLE-DOSE (10139-063-10)

NDC Information of Fluorouracil

NDC Code 10139-063-11
Proprietary Name Fluorouracil
Package Description 10 VIAL, SINGLE-DOSE in 1 CARTON (10139-063-11) > 10 mL in 1 VIAL, SINGLE-DOSE (10139-063-10)
Product NDC 10139-063
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Fluorouracil
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 20120830
Marketing Category Name ANDA
Labeler Name GeneraMedix
Substance Name FLUOROURACIL
Strength Number 50
Strength Unit mg/mL
Pharmaceutical Classes Nucleic Acid Synthesis Inhibitors [MoA],Nucleoside Metabolic Inhibitor [EPC]

Complete Information of Fluorouracil


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