MEFOXIN - 67457-216-50 - (cefoxitin sodium)

Alphabetical Index


Drug Information of MEFOXIN

Product NDC: 67457-216
Proprietary Name: MEFOXIN
Non Proprietary Name: cefoxitin sodium
Active Ingredient(s): 2    g/50mL & nbsp;   cefoxitin sodium
Administration Route(s): INTRAVENOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of MEFOXIN

Product NDC: 67457-216
Labeler Name: Bioniche Pharma USA LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA063182
Marketing Category: ANDA
Start Marketing Date: 20110222

Package Information of MEFOXIN

Package NDC: 67457-216-50
Package Description: 24 BAG in 1 BOX (67457-216-50) > 50 mL in 1 BAG

NDC Information of MEFOXIN

NDC Code 67457-216-50
Proprietary Name MEFOXIN
Package Description 24 BAG in 1 BOX (67457-216-50) > 50 mL in 1 BAG
Product NDC 67457-216
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name cefoxitin sodium
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 20110222
Marketing Category Name ANDA
Labeler Name Bioniche Pharma USA LLC
Substance Name CEFOXITIN SODIUM
Strength Number 2
Strength Unit g/50mL
Pharmaceutical Classes Cephalosporin Antibacterial [EPC],Cephalosporins [Chemical/Ingredient]

Complete Information of MEFOXIN


General Information