CEFOTAXIME - 55648-948-02 - (CEFOTAXIME)

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Drug Information of CEFOTAXIME

Product NDC: 55648-948
Proprietary Name: CEFOTAXIME
Non Proprietary Name: CEFOTAXIME
Active Ingredient(s): 2    g/mL & 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: 55648-948
Labeler Name: WOCKHARDT LIMITED
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA065197
Marketing Category: ANDA
Start Marketing Date: 20080620

Package Information of CEFOTAXIME

Package NDC: 55648-948-02
Package Description: 10 CARTON in 1 CARTON (55648-948-02) > 1 VIAL, SINGLE-DOSE in 1 CARTON (55648-948-01) > 20 mL in 1 VIAL, SINGLE-DOSE

NDC Information of CEFOTAXIME

NDC Code 55648-948-02
Proprietary Name CEFOTAXIME
Package Description 10 CARTON in 1 CARTON (55648-948-02) > 1 VIAL, SINGLE-DOSE in 1 CARTON (55648-948-01) > 20 mL in 1 VIAL, SINGLE-DOSE
Product NDC 55648-948
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name CEFOTAXIME
Dosage Form Name INJECTION, POWDER, FOR SOLUTION
Route Name INTRAMUSCULAR; INTRAVENOUS
Start Marketing Date 20080620
Marketing Category Name ANDA
Labeler Name WOCKHARDT LIMITED
Substance Name CEFOTAXIME SODIUM
Strength Number 2
Strength Unit g/mL
Pharmaceutical Classes Cephalosporin Antibacterial [EPC],Cephalosporins [Chemical/Ingredient]

Complete Information of CEFOTAXIME


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