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Carboplatin - 55390-151-01 - (Carboplatin)

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Drug Information of Carboplatin

Product NDC: 55390-151
Proprietary Name: Carboplatin
Non Proprietary Name: Carboplatin
Active Ingredient(s): 150    mg/15mL & nbsp;   Carboplatin
Administration Route(s): INTRAVENOUS
Dosage Form(s): INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Carboplatin

Product NDC: 55390-151
Labeler Name: Bedford Laboratories
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076099
Marketing Category: ANDA
Start Marketing Date: 20060117

Package Information of Carboplatin

Package NDC: 55390-151-01
Package Description: 1 VIAL in 1 BOX, UNIT-DOSE (55390-151-01) > 15 mL in 1 VIAL

NDC Information of Carboplatin

NDC Code 55390-151-01
Proprietary Name Carboplatin
Package Description 1 VIAL in 1 BOX, UNIT-DOSE (55390-151-01) > 15 mL in 1 VIAL
Product NDC 55390-151
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Carboplatin
Dosage Form Name INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 20060117
Marketing Category Name ANDA
Labeler Name Bedford Laboratories
Substance Name CARBOPLATIN
Strength Number 150
Strength Unit mg/15mL
Pharmaceutical Classes Platinum-based Drug [EPC],Platinum-containing Compounds [Chemical/Ingredient]

Complete Information of Carboplatin


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