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Dacarbazine - 55390-090-10 - (Dacarbazine)

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Drug Information of Dacarbazine

Product NDC: 55390-090
Proprietary Name: Dacarbazine
Non Proprietary Name: Dacarbazine
Active Ingredient(s): 200    mg/20mL & nbsp;   Dacarbazine
Administration Route(s): INTRAVENOUS
Dosage Form(s): INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Dacarbazine

Product NDC: 55390-090
Labeler Name: Bedford Laboratories
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075812
Marketing Category: ANDA
Start Marketing Date: 20010808

Package Information of Dacarbazine

Package NDC: 55390-090-10
Package Description: 10 VIAL in 1 BOX (55390-090-10) > 20 mL in 1 VIAL

NDC Information of Dacarbazine

NDC Code 55390-090-10
Proprietary Name Dacarbazine
Package Description 10 VIAL in 1 BOX (55390-090-10) > 20 mL in 1 VIAL
Product NDC 55390-090
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Dacarbazine
Dosage Form Name INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 20010808
Marketing Category Name ANDA
Labeler Name Bedford Laboratories
Substance Name DACARBAZINE
Strength Number 200
Strength Unit mg/20mL
Pharmaceutical Classes Alkylating Activity [MoA],Alkylating Drug [EPC]

Complete Information of Dacarbazine


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