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Fluorouracil - 66758-044-03 - (Fluorouracil)

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Drug Information of Fluorouracil

Product NDC: 66758-044
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: 66758-044
Labeler Name: Sandoz Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040772
Marketing Category: ANDA
Start Marketing Date: 20080910

Package Information of Fluorouracil

Package NDC: 66758-044-03
Package Description: 10 VIAL, SINGLE-USE in 1 CARTON (66758-044-03) > 10 mL in 1 VIAL, SINGLE-USE (66758-044-01)

NDC Information of Fluorouracil

NDC Code 66758-044-03
Proprietary Name Fluorouracil
Package Description 10 VIAL, SINGLE-USE in 1 CARTON (66758-044-03) > 10 mL in 1 VIAL, SINGLE-USE (66758-044-01)
Product NDC 66758-044
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Fluorouracil
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 20080910
Marketing Category Name ANDA
Labeler Name Sandoz Inc
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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