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Mitoxantrone - 55390-085-01 - (Mitoxantrone hydrochloride)

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Drug Information of Mitoxantrone

Product NDC: 55390-085
Proprietary Name: Mitoxantrone
Non Proprietary Name: Mitoxantrone hydrochloride
Active Ingredient(s): 2    mg/mL & nbsp;   Mitoxantrone hydrochloride
Administration Route(s): INTRAVENOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Mitoxantrone

Product NDC: 55390-085
Labeler Name: Bedford Laboratories
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076611
Marketing Category: ANDA
Start Marketing Date: 20060411

Package Information of Mitoxantrone

Package NDC: 55390-085-01
Package Description: 1 VIAL, MULTI-DOSE in 1 BOX (55390-085-01) > 15 mL in 1 VIAL, MULTI-DOSE

NDC Information of Mitoxantrone

NDC Code 55390-085-01
Proprietary Name Mitoxantrone
Package Description 1 VIAL, MULTI-DOSE in 1 BOX (55390-085-01) > 15 mL in 1 VIAL, MULTI-DOSE
Product NDC 55390-085
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Mitoxantrone hydrochloride
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 20060411
Marketing Category Name ANDA
Labeler Name Bedford Laboratories
Substance Name MITOXANTRONE
Strength Number 2
Strength Unit mg/mL
Pharmaceutical Classes Topoisomerase Inhibitor [EPC],Topoisomerase Inhibitors [MoA]

Complete Information of Mitoxantrone


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