Rifampin - 55390-123-01 - (Rifampin)

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Drug Information of Rifampin

Product NDC: 55390-123
Proprietary Name: Rifampin
Non Proprietary Name: Rifampin
Active Ingredient(s): 600    mg/10mL & nbsp;   Rifampin
Administration Route(s): INTRAVENOUS
Dosage Form(s): INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Rifampin

Product NDC: 55390-123
Labeler Name: Bedford Laboratories
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA064217
Marketing Category: ANDA
Start Marketing Date: 20020218

Package Information of Rifampin

Package NDC: 55390-123-01
Package Description: 1 VIAL in 1 BOX, UNIT-DOSE (55390-123-01) > 10 mL in 1 VIAL

NDC Information of Rifampin

NDC Code 55390-123-01
Proprietary Name Rifampin
Package Description 1 VIAL in 1 BOX, UNIT-DOSE (55390-123-01) > 10 mL in 1 VIAL
Product NDC 55390-123
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Rifampin
Dosage Form Name INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 20020218
Marketing Category Name ANDA
Labeler Name Bedford Laboratories
Substance Name RIFAMPIN
Strength Number 600
Strength Unit mg/10mL
Pharmaceutical Classes Rifamycin Antibacterial [EPC],Rifamycins [Chemical/Ingredient]

Complete Information of Rifampin


General Information