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Fluorouracil - 52549-4118-2 - (Fluorouracil)

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Drug Information of Fluorouracil

Product NDC: 52549-4118
Proprietary Name: Fluorouracil
Non Proprietary Name: Fluorouracil
Active Ingredient(s): 50    mg/g & nbsp;   Fluorouracil
Administration Route(s): TOPICAL
Dosage Form(s): CREAM
Coding System: National Drug Codes(NDC)

Labeler Information of Fluorouracil

Product NDC: 52549-4118
Labeler Name: Taro Pharmaceutical Industries Ltd.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090368
Marketing Category: ANDA
Start Marketing Date: 20100305

Package Information of Fluorouracil

Package NDC: 52549-4118-2
Package Description: 1 TUBE in 1 CARTON (52549-4118-2) > 25 g in 1 TUBE

NDC Information of Fluorouracil

NDC Code 52549-4118-2
Proprietary Name Fluorouracil
Package Description 1 TUBE in 1 CARTON (52549-4118-2) > 25 g in 1 TUBE
Product NDC 52549-4118
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Fluorouracil
Dosage Form Name CREAM
Route Name TOPICAL
Start Marketing Date 20100305
Marketing Category Name ANDA
Labeler Name Taro Pharmaceutical Industries Ltd.
Substance Name FLUOROURACIL
Strength Number 50
Strength Unit mg/g
Pharmaceutical Classes Nucleic Acid Synthesis Inhibitors [MoA],Nucleoside Metabolic Inhibitor [EPC]

Complete Information of Fluorouracil


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