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Carboplatin - 0703-3249-11 - (Carboplatin)

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Drug Information of Carboplatin

Product NDC: 0703-3249
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: 0703-3249
Labeler Name: Teva Parenteral Medicines, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077139
Marketing Category: ANDA
Start Marketing Date: 20051117

Package Information of Carboplatin

Package NDC: 0703-3249-11
Package Description: 1 VIAL, MULTI-DOSE in 1 CARTON (0703-3249-11) > 60 mL in 1 VIAL, MULTI-DOSE

NDC Information of Carboplatin

NDC Code 0703-3249-11
Proprietary Name Carboplatin
Package Description 1 VIAL, MULTI-DOSE in 1 CARTON (0703-3249-11) > 60 mL in 1 VIAL, MULTI-DOSE
Product NDC 0703-3249
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Carboplatin
Dosage Form Name INJECTION
Route Name INTRAVENOUS
Start Marketing Date 20051117
Marketing Category Name ANDA
Labeler Name Teva Parenteral Medicines, 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


General Information