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Oxaliplatin - 0703-3985-01 - (Oxaliplatin)

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Drug Information of Oxaliplatin

Product NDC: 0703-3985
Proprietary Name: Oxaliplatin
Non Proprietary Name: Oxaliplatin
Active Ingredient(s): 50    mg/10mL & nbsp;   Oxaliplatin
Administration Route(s): INTRAVENOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Oxaliplatin

Product NDC: 0703-3985
Labeler Name: Teva Parenteral Medicines, Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA022160
Marketing Category: NDA
Start Marketing Date: 20090811

Package Information of Oxaliplatin

Package NDC: 0703-3985-01
Package Description: 1 VIAL, SINGLE-USE in 1 CARTON (0703-3985-01) > 10 mL in 1 VIAL, SINGLE-USE

NDC Information of Oxaliplatin

NDC Code 0703-3985-01
Proprietary Name Oxaliplatin
Package Description 1 VIAL, SINGLE-USE in 1 CARTON (0703-3985-01) > 10 mL in 1 VIAL, SINGLE-USE
Product NDC 0703-3985
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Oxaliplatin
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 20090811
Marketing Category Name NDA
Labeler Name Teva Parenteral Medicines, Inc
Substance Name OXALIPLATIN
Strength Number 50
Strength Unit mg/10mL
Pharmaceutical Classes Platinum-based Drug [EPC],Platinum-containing Compounds [Chemical/Ingredient]

Complete Information of Oxaliplatin


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