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Dacarbazine - 63323-127-10 - (DACARBAZINE)

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Drug Information of Dacarbazine

Product NDC: 63323-127
Proprietary Name: Dacarbazine
Non Proprietary Name: DACARBAZINE
Active Ingredient(s): 10    mg/mL & nbsp;   DACARBAZINE
Administration Route(s): INTRAVENOUS
Dosage Form(s): INJECTION, POWDER, FOR SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Dacarbazine

Product NDC: 63323-127
Labeler Name: APP Pharmaceuticals, LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075371
Marketing Category: ANDA
Start Marketing Date: 20010907

Package Information of Dacarbazine

Package NDC: 63323-127-10
Package Description: 10 VIAL, SINGLE-DOSE in 1 TRAY (63323-127-10) > 10 mL in 1 VIAL, SINGLE-DOSE

NDC Information of Dacarbazine

NDC Code 63323-127-10
Proprietary Name Dacarbazine
Package Description 10 VIAL, SINGLE-DOSE in 1 TRAY (63323-127-10) > 10 mL in 1 VIAL, SINGLE-DOSE
Product NDC 63323-127
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name DACARBAZINE
Dosage Form Name INJECTION, POWDER, FOR SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 20010907
Marketing Category Name ANDA
Labeler Name APP Pharmaceuticals, LLC
Substance Name DACARBAZINE
Strength Number 10
Strength Unit mg/mL
Pharmaceutical Classes Alkylating Activity [MoA],Alkylating Drug [EPC]

Complete Information of Dacarbazine


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