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Ceftriaxone - 63323-346-10 - (Ceftriaxone)

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Drug Information of Ceftriaxone

Product NDC: 63323-346
Proprietary Name: Ceftriaxone
Non Proprietary Name: Ceftriaxone
Active Ingredient(s): 1    g/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: 63323-346
Labeler Name: APP Pharmaceuticals , LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA065329
Marketing Category: ANDA
Start Marketing Date: 20110620

Package Information of Ceftriaxone

Package NDC: 63323-346-10
Package Description: 25 VIAL in 1 CARTON (63323-346-10) > 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL

NDC Information of Ceftriaxone

NDC Code 63323-346-10
Proprietary Name Ceftriaxone
Package Description 25 VIAL in 1 CARTON (63323-346-10) > 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL
Product NDC 63323-346
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Ceftriaxone
Dosage Form Name INJECTION, POWDER, FOR SOLUTION
Route Name INTRAMUSCULAR; INTRAVENOUS
Start Marketing Date 20110620
Marketing Category Name ANDA
Labeler Name APP Pharmaceuticals , LLC
Substance Name CEFTRIAXONE SODIUM
Strength Number 1
Strength Unit g/1
Pharmaceutical Classes Cephalosporin Antibacterial [EPC],Cephalosporins [Chemical/Ingredient]

Complete Information of Ceftriaxone


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