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OXALIPLATIN - 0069-0067-01 - (OXALIPLATIN)

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Drug Information of OXALIPLATIN

Product NDC: 0069-0067
Proprietary Name: OXALIPLATIN
Non Proprietary Name: OXALIPLATIN
Active Ingredient(s): 50    mg/10mL & nbsp;   OXALIPLATIN
Administration Route(s): INTRAVENOUS
Dosage Form(s): POWDER, FOR SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of OXALIPLATIN

Product NDC: 0069-0067
Labeler Name: Pfizer Laboratories Div Pfizer Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA200979
Marketing Category: ANDA
Start Marketing Date: 20120809

Package Information of OXALIPLATIN

Package NDC: 0069-0067-01
Package Description: 10 mL in 1 VIAL (0069-0067-01)

NDC Information of OXALIPLATIN

NDC Code 0069-0067-01
Proprietary Name OXALIPLATIN
Package Description 10 mL in 1 VIAL (0069-0067-01)
Product NDC 0069-0067
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name OXALIPLATIN
Dosage Form Name POWDER, FOR SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 20120809
Marketing Category Name ANDA
Labeler Name Pfizer Laboratories Div Pfizer 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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