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Ceftriaxone - 0143-9768-46 - (Ceftriaxone)

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Drug Information of Ceftriaxone

Product NDC: 0143-9768
Proprietary Name: Ceftriaxone
Non Proprietary Name: Ceftriaxone
Active Ingredient(s): 10    g/100mL & nbsp;   Ceftriaxone
Administration Route(s): INTRAVENOUS
Dosage Form(s): POWDER, FOR SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Ceftriaxone

Product NDC: 0143-9768
Labeler Name: West-ward Pharmaceutical Corp
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA065328
Marketing Category: NDA
Start Marketing Date: 20090806

Package Information of Ceftriaxone

Package NDC: 0143-9768-46
Package Description: 1 VIAL in 1 BOX (0143-9768-46) > 100 mL in 1 VIAL (0143-9768-01)

NDC Information of Ceftriaxone

NDC Code 0143-9768-46
Proprietary Name Ceftriaxone
Package Description 1 VIAL in 1 BOX (0143-9768-46) > 100 mL in 1 VIAL (0143-9768-01)
Product NDC 0143-9768
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Ceftriaxone
Dosage Form Name POWDER, FOR SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 20090806
Marketing Category Name NDA
Labeler Name West-ward Pharmaceutical Corp
Substance Name CEFTRIAXONE SODIUM
Strength Number 10
Strength Unit g/100mL
Pharmaceutical Classes Cephalosporin Antibacterial [EPC],Cephalosporins [Chemical/Ingredient]

Complete Information of Ceftriaxone


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