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Carboplatin - 63323-172-05 - (Carboplatin)

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Drug Information of Carboplatin

Product NDC: 63323-172
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: 63323-172
Labeler Name: APP Pharmaceuticals, LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077432
Marketing Category: ANDA
Start Marketing Date: 20090915

Package Information of Carboplatin

Package NDC: 63323-172-05
Package Description: 1 VIAL in 1 BOX (63323-172-05) > 5 mL in 1 VIAL

NDC Information of Carboplatin

NDC Code 63323-172-05
Proprietary Name Carboplatin
Package Description 1 VIAL in 1 BOX (63323-172-05) > 5 mL in 1 VIAL
Product NDC 63323-172
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Carboplatin
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 20090915
Marketing Category Name ANDA
Labeler Name APP Pharmaceuticals, LLC
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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