Cefotaxime - 0143-9933-25 - (Cefotaxime)

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Drug Information of Cefotaxime

Product NDC: 0143-9933
Proprietary Name: Cefotaxime
Non Proprietary Name: Cefotaxime
Active Ingredient(s): 2    g/1 & nbsp;   Cefotaxime
Administration Route(s): INTRAMUSCULAR; INTRAVENOUS
Dosage Form(s): INJECTION, POWDER, FOR SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Cefotaxime

Product NDC: 0143-9933
Labeler Name: West-ward Pharmaceutical Corp
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA065071
Marketing Category: ANDA
Start Marketing Date: 20021120

Package Information of Cefotaxime

Package NDC: 0143-9933-25
Package Description: 25 VIAL in 1 PACKAGE (0143-9933-25) > 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL (0143-9933-01)

NDC Information of Cefotaxime

NDC Code 0143-9933-25
Proprietary Name Cefotaxime
Package Description 25 VIAL in 1 PACKAGE (0143-9933-25) > 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL (0143-9933-01)
Product NDC 0143-9933
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Cefotaxime
Dosage Form Name INJECTION, POWDER, FOR SOLUTION
Route Name INTRAMUSCULAR; INTRAVENOUS
Start Marketing Date 20021120
Marketing Category Name ANDA
Labeler Name West-ward Pharmaceutical Corp
Substance Name CEFOTAXIME SODIUM
Strength Number 2
Strength Unit g/1
Pharmaceutical Classes Cephalosporin Antibacterial [EPC],Cephalosporins [Chemical/Ingredient]

Complete Information of Cefotaxime


General Information