Mitomycin - 55390-251-01 - (Mitomycin)

Alphabetical Index


Drug Information of Mitomycin

Product NDC: 55390-251
Proprietary Name: Mitomycin
Non Proprietary Name: Mitomycin
Active Ingredient(s): 10    mg/20mL & nbsp;   Mitomycin
Administration Route(s): INTRAVENOUS
Dosage Form(s): INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Mitomycin

Product NDC: 55390-251
Labeler Name: Bedford Laboratories
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA064117
Marketing Category: ANDA
Start Marketing Date: 19960501

Package Information of Mitomycin

Package NDC: 55390-251-01
Package Description: 1 VIAL in 1 BOX, UNIT-DOSE (55390-251-01) > 10 mL in 1 VIAL

NDC Information of Mitomycin

NDC Code 55390-251-01
Proprietary Name Mitomycin
Package Description 1 VIAL in 1 BOX, UNIT-DOSE (55390-251-01) > 10 mL in 1 VIAL
Product NDC 55390-251
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Mitomycin
Dosage Form Name INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 19960501
Marketing Category Name ANDA
Labeler Name Bedford Laboratories
Substance Name MITOMYCIN
Strength Number 10
Strength Unit mg/20mL
Pharmaceutical Classes Alkylating Activity [MoA],Alkylating Drug [EPC]

Complete Information of Mitomycin


General Information