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Carboplatin - 61703-339-50 - (Carboplatin)

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Drug Information of Carboplatin

Product NDC: 61703-339
Proprietary Name: Carboplatin
Non Proprietary Name: Carboplatin
Active Ingredient(s): 10    mg/mL & nbsp;   Carboplatin
Administration Route(s): INTRAVENOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Carboplatin

Product NDC: 61703-339
Labeler Name: Hospira Worldwide, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076517
Marketing Category: ANDA
Start Marketing Date: 20091217

Package Information of Carboplatin

Package NDC: 61703-339-50
Package Description: 1 VIAL, MULTI-DOSE in 1 CARTON (61703-339-50) > 45 mL in 1 VIAL, MULTI-DOSE

NDC Information of Carboplatin

NDC Code 61703-339-50
Proprietary Name Carboplatin
Package Description 1 VIAL, MULTI-DOSE in 1 CARTON (61703-339-50) > 45 mL in 1 VIAL, MULTI-DOSE
Product NDC 61703-339
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Carboplatin
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 20091217
Marketing Category Name ANDA
Labeler Name Hospira Worldwide, Inc.
Substance Name CARBOPLATIN
Strength Number 10
Strength Unit mg/mL
Pharmaceutical Classes Platinum-based Drug [EPC],Platinum-containing Compounds [Chemical/Ingredient]

Complete Information of Carboplatin


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