Cefotetan - 63323-396-61 - (CEFOTETAN DISODIUM)

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Drug Information of Cefotetan

Product NDC: 63323-396
Proprietary Name: Cefotetan
Non Proprietary Name: CEFOTETAN DISODIUM
Active Ingredient(s): 10    g/1 & nbsp;   CEFOTETAN DISODIUM
Administration Route(s): INTRAVENOUS
Dosage Form(s): INJECTION, POWDER, FOR SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Cefotetan

Product NDC: 63323-396
Labeler Name: APP Pharmaceuticals, LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA065375
Marketing Category: ANDA
Start Marketing Date: 20091203

Package Information of Cefotetan

Package NDC: 63323-396-61
Package Description: 1 VIAL in 1 BOX (63323-396-61) > 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL

NDC Information of Cefotetan

NDC Code 63323-396-61
Proprietary Name Cefotetan
Package Description 1 VIAL in 1 BOX (63323-396-61) > 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL
Product NDC 63323-396
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name CEFOTETAN DISODIUM
Dosage Form Name INJECTION, POWDER, FOR SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 20091203
Marketing Category Name ANDA
Labeler Name APP Pharmaceuticals, LLC
Substance Name CEFOTETAN DISODIUM
Strength Number 10
Strength Unit g/1
Pharmaceutical Classes Cephalosporin Antibacterial [EPC],Cephalosporins [Chemical/Ingredient]

Complete Information of Cefotetan


General Information