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Carboplatin - 55390-156-01 - (Carboplatin)

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Drug Information of Carboplatin

Product NDC: 55390-156
Proprietary Name: Carboplatin
Non Proprietary Name: Carboplatin
Active Ingredient(s): 10    mg/mL & nbsp;   Carboplatin
Administration Route(s): INTRAVENOUS
Dosage Form(s): INJECTION
Coding System: National Drug Codes(NDC)

Labeler Information of Carboplatin

Product NDC: 55390-156
Labeler Name: Bedford Laboratories
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077244
Marketing Category: ANDA
Start Marketing Date: 20041014

Package Information of Carboplatin

Package NDC: 55390-156-01
Package Description: 1 VIAL in 1 BOX, UNIT-DOSE (55390-156-01) > 60 mL in 1 VIAL

NDC Information of Carboplatin

NDC Code 55390-156-01
Proprietary Name Carboplatin
Package Description 1 VIAL in 1 BOX, UNIT-DOSE (55390-156-01) > 60 mL in 1 VIAL
Product NDC 55390-156
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Carboplatin
Dosage Form Name INJECTION
Route Name INTRAVENOUS
Start Marketing Date 20041014
Marketing Category Name ANDA
Labeler Name Bedford Laboratories
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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