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oxaliplatin - 63323-650-27 - (oxaliplatin)

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Drug Information of oxaliplatin

Product NDC: 63323-650
Proprietary Name: oxaliplatin
Non Proprietary Name: oxaliplatin
Active Ingredient(s): 5    mg/mL & nbsp;   oxaliplatin
Administration Route(s): INTRAVENOUS
Dosage Form(s): INJECTION, SOLUTION, CONCENTRATE
Coding System: National Drug Codes(NDC)

Labeler Information of oxaliplatin

Product NDC: 63323-650
Labeler Name: APP Pharmaceuticals, LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078811
Marketing Category: ANDA
Start Marketing Date: 20100611

Package Information of oxaliplatin

Package NDC: 63323-650-27
Package Description: 10 BOX in 1 CARTON (63323-650-27) > 1 VIAL in 1 BOX > 20 mL in 1 VIAL

NDC Information of oxaliplatin

NDC Code 63323-650-27
Proprietary Name oxaliplatin
Package Description 10 BOX in 1 CARTON (63323-650-27) > 1 VIAL in 1 BOX > 20 mL in 1 VIAL
Product NDC 63323-650
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name oxaliplatin
Dosage Form Name INJECTION, SOLUTION, CONCENTRATE
Route Name INTRAVENOUS
Start Marketing Date 20100611
Marketing Category Name ANDA
Labeler Name APP Pharmaceuticals, LLC
Substance Name OXALIPLATIN
Strength Number 5
Strength Unit mg/mL
Pharmaceutical Classes Platinum-based Drug [EPC],Platinum-containing Compounds [Chemical/Ingredient]

Complete Information of oxaliplatin


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