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Platinol-AQ - 61126-004-01 - (cisplatin)

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Drug Information of Platinol-AQ

Product NDC: 61126-004
Proprietary Name: Platinol-AQ
Non Proprietary Name: cisplatin
Active Ingredient(s): 1    mg/mL & nbsp;   cisplatin
Administration Route(s): INTRAVENOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Platinol-AQ

Product NDC: 61126-004
Labeler Name: Corden Pharma Latina S.p.A.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA018057
Marketing Category: NDA
Start Marketing Date: 20120113

Package Information of Platinol-AQ

Package NDC: 61126-004-01
Package Description: 1 VIAL, MULTI-DOSE in 1 CARTON (61126-004-01) > 50 mL in 1 VIAL, MULTI-DOSE

NDC Information of Platinol-AQ

NDC Code 61126-004-01
Proprietary Name Platinol-AQ
Package Description 1 VIAL, MULTI-DOSE in 1 CARTON (61126-004-01) > 50 mL in 1 VIAL, MULTI-DOSE
Product NDC 61126-004
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name cisplatin
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 20120113
Marketing Category Name NDA
Labeler Name Corden Pharma Latina S.p.A.
Substance Name CISPLATIN
Strength Number 1
Strength Unit mg/mL
Pharmaceutical Classes Platinum-based Drug [EPC],Platinum-containing Compounds [Chemical/Ingredient]

Complete Information of Platinol-AQ


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