Rocephin - 0004-1963-01 - (ceftriaxone sodium)

Alphabetical Index


Drug Information of Rocephin

Product NDC: 0004-1963
Proprietary Name: Rocephin
Non Proprietary Name: ceftriaxone sodium
Active Ingredient(s): 500    mg/1 & nbsp;   ceftriaxone sodium
Administration Route(s): INTRAMUSCULAR; INTRAVENOUS
Dosage Form(s): INJECTION, POWDER, FOR SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Rocephin

Product NDC: 0004-1963
Labeler Name: Genentech, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA063239
Marketing Category: ANDA
Start Marketing Date: 19930813

Package Information of Rocephin

Package NDC: 0004-1963-01
Package Description: 10 VIAL, GLASS in 1 BOX (0004-1963-01) > 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, GLASS

NDC Information of Rocephin

NDC Code 0004-1963-01
Proprietary Name Rocephin
Package Description 10 VIAL, GLASS in 1 BOX (0004-1963-01) > 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, GLASS
Product NDC 0004-1963
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name ceftriaxone sodium
Dosage Form Name INJECTION, POWDER, FOR SOLUTION
Route Name INTRAMUSCULAR; INTRAVENOUS
Start Marketing Date 19930813
Marketing Category Name ANDA
Labeler Name Genentech, Inc.
Substance Name CEFTRIAXONE SODIUM
Strength Number 500
Strength Unit mg/1
Pharmaceutical Classes Cephalosporin Antibacterial [EPC],Cephalosporins [Chemical/Ingredient]

Complete Information of Rocephin


General Information