CEFOTAXIME - 64679-986-03 - (CEFOTAXIME)

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Drug Information of CEFOTAXIME

Product NDC: 64679-986
Proprietary Name: CEFOTAXIME
Non Proprietary Name: CEFOTAXIME
Active Ingredient(s): 1    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: 64679-986
Labeler Name: WOCKHARDT USA LLC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA065197
Marketing Category: ANDA
Start Marketing Date: 20060829

Package Information of CEFOTAXIME

Package NDC: 64679-986-03
Package Description: 25 CARTON in 1 CARTON (64679-986-03) > 1 INJECTION, POWDER, FOR SOLUTION in 1 CARTON (64679-986-01)

NDC Information of CEFOTAXIME

NDC Code 64679-986-03
Proprietary Name CEFOTAXIME
Package Description 25 CARTON in 1 CARTON (64679-986-03) > 1 INJECTION, POWDER, FOR SOLUTION in 1 CARTON (64679-986-01)
Product NDC 64679-986
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name CEFOTAXIME
Dosage Form Name INJECTION, POWDER, FOR SOLUTION
Route Name INTRAMUSCULAR; INTRAVENOUS
Start Marketing Date 20060829
Marketing Category Name ANDA
Labeler Name WOCKHARDT USA LLC.
Substance Name CEFOTAXIME SODIUM
Strength Number 1
Strength Unit g/1
Pharmaceutical Classes Cephalosporin Antibacterial [EPC],Cephalosporins [Chemical/Ingredient]

Complete Information of CEFOTAXIME


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