ADRUCIL - 0703-3015-13 - (fluorouracil)

Alphabetical Index


Drug Information of ADRUCIL

Product NDC: 0703-3015
Proprietary Name: ADRUCIL
Non Proprietary Name: fluorouracil
Active Ingredient(s): 50    mg/mL & nbsp;   fluorouracil
Administration Route(s): INTRAVENOUS
Dosage Form(s): INJECTION
Coding System: National Drug Codes(NDC)

Labeler Information of ADRUCIL

Product NDC: 0703-3015
Labeler Name: Teva Parenteral Medicines, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040333
Marketing Category: ANDA
Start Marketing Date: 20031001

Package Information of ADRUCIL

Package NDC: 0703-3015-13
Package Description: 10 VIAL in 1 TRAY (0703-3015-13) > 10 mL in 1 VIAL (0703-3015-11)

NDC Information of ADRUCIL

NDC Code 0703-3015-13
Proprietary Name ADRUCIL
Package Description 10 VIAL in 1 TRAY (0703-3015-13) > 10 mL in 1 VIAL (0703-3015-11)
Product NDC 0703-3015
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name fluorouracil
Dosage Form Name INJECTION
Route Name INTRAVENOUS
Start Marketing Date 20031001
Marketing Category Name ANDA
Labeler Name Teva Parenteral Medicines, 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 ADRUCIL


General Information