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cefuroxime axetil - 68180-303-20 - (cefuroxime axetil)

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Drug Information of cefuroxime axetil

Product NDC: 68180-303
Proprietary Name: cefuroxime axetil
Non Proprietary Name: cefuroxime axetil
Active Ingredient(s): 500    mg/1 & nbsp;   cefuroxime axetil
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of cefuroxime axetil

Product NDC: 68180-303
Labeler Name: LUPIN PHARMACEUTICALS INC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA065135
Marketing Category: ANDA
Start Marketing Date: 20030725

Package Information of cefuroxime axetil

Package NDC: 68180-303-20
Package Description: 20 TABLET in 1 BOTTLE (68180-303-20)

NDC Information of cefuroxime axetil

NDC Code 68180-303-20
Proprietary Name cefuroxime axetil
Package Description 20 TABLET in 1 BOTTLE (68180-303-20)
Product NDC 68180-303
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name cefuroxime axetil
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20030725
Marketing Category Name ANDA
Labeler Name LUPIN PHARMACEUTICALS INC
Substance Name CEFUROXIME AXETIL
Strength Number 500
Strength Unit mg/1
Pharmaceutical Classes Cephalosporin Antibacterial [EPC],Cephalosporins [Chemical/Ingredient]

Complete Information of cefuroxime axetil


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