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Fluorouracil - 63323-117-61 - (FLUOROURACIL)

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Drug Information of Fluorouracil

Product NDC: 63323-117
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: 63323-117
Labeler Name: APP Pharmaceuticals, LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040278
Marketing Category: ANDA
Start Marketing Date: 20000712

Package Information of Fluorouracil

Package NDC: 63323-117-61
Package Description: 1 VIAL, PHARMACY BULK PACKAGE in 1 CARTON (63323-117-61) > 100 mL in 1 VIAL, PHARMACY BULK PACKAGE

NDC Information of Fluorouracil

NDC Code 63323-117-61
Proprietary Name Fluorouracil
Package Description 1 VIAL, PHARMACY BULK PACKAGE in 1 CARTON (63323-117-61) > 100 mL in 1 VIAL, PHARMACY BULK PACKAGE
Product NDC 63323-117
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name FLUOROURACIL
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 20000712
Marketing Category Name ANDA
Labeler Name APP Pharmaceuticals, LLC
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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