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CEFTRIAXONE - 68180-611-01 - (CEFTRIAXONE)

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Drug Information of CEFTRIAXONE

Product NDC: 68180-611
Proprietary Name: CEFTRIAXONE
Non Proprietary Name: CEFTRIAXONE
Active Ingredient(s): 250    mg/1 & nbsp;   CEFTRIAXONE
Administration Route(s): INTRAMUSCULAR; INTRAVENOUS
Dosage Form(s): INJECTION, POWDER, FOR SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of CEFTRIAXONE

Product NDC: 68180-611
Labeler Name: LUPIN PHARMACEUTICALS INC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA065125
Marketing Category: ANDA
Start Marketing Date: 20030930

Package Information of CEFTRIAXONE

Package NDC: 68180-611-01
Package Description: 1 INJECTION, POWDER, FOR SOLUTION in 1 BOX (68180-611-01)

NDC Information of CEFTRIAXONE

NDC Code 68180-611-01
Proprietary Name CEFTRIAXONE
Package Description 1 INJECTION, POWDER, FOR SOLUTION in 1 BOX (68180-611-01)
Product NDC 68180-611
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name CEFTRIAXONE
Dosage Form Name INJECTION, POWDER, FOR SOLUTION
Route Name INTRAMUSCULAR; INTRAVENOUS
Start Marketing Date 20030930
Marketing Category Name ANDA
Labeler Name LUPIN PHARMACEUTICALS INC
Substance Name CEFTRIAXONE SODIUM
Strength Number 250
Strength Unit mg/1
Pharmaceutical Classes Cephalosporin Antibacterial [EPC],Cephalosporins [Chemical/Ingredient]

Complete Information of CEFTRIAXONE


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