Rifadin IV - 0068-0597-01 - (rifampin)

Alphabetical Index


Drug Information of Rifadin IV

Product NDC: 0068-0597
Proprietary Name: Rifadin IV
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 Rifadin IV

Product NDC: 0068-0597
Labeler Name: Sanofi-Aventis U.S. LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA050627
Marketing Category: NDA
Start Marketing Date: 19890525

Package Information of Rifadin IV

Package NDC: 0068-0597-01
Package Description: 10 mL in 1 VIAL, GLASS (0068-0597-01)

NDC Information of Rifadin IV

NDC Code 0068-0597-01
Proprietary Name Rifadin IV
Package Description 10 mL in 1 VIAL, GLASS (0068-0597-01)
Product NDC 0068-0597
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name rifampin
Dosage Form Name INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 19890525
Marketing Category Name NDA
Labeler Name Sanofi-Aventis U.S. LLC
Substance Name RIFAMPIN
Strength Number 600
Strength Unit mg/10mL
Pharmaceutical Classes Rifamycin Antibacterial [EPC],Rifamycins [Chemical/Ingredient]

Complete Information of Rifadin IV


General Information