SUPRAX - 27437-206-05 - (cefixime)

Alphabetical Index


Drug Information of SUPRAX

Product NDC: 27437-206
Proprietary Name: SUPRAX
Non Proprietary Name: cefixime
Active Ingredient(s): 200    mg/5mL & nbsp;   cefixime
Administration Route(s): ORAL
Dosage Form(s): POWDER, FOR SUSPENSION
Coding System: National Drug Codes(NDC)

Labeler Information of SUPRAX

Product NDC: 27437-206
Labeler Name: LUPIN PHARMA
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA065355
Marketing Category: ANDA
Start Marketing Date: 20070601

Package Information of SUPRAX

Package NDC: 27437-206-05
Package Description: 25 mL in 1 BOTTLE (27437-206-05)

NDC Information of SUPRAX

NDC Code 27437-206-05
Proprietary Name SUPRAX
Package Description 25 mL in 1 BOTTLE (27437-206-05)
Product NDC 27437-206
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name cefixime
Dosage Form Name POWDER, FOR SUSPENSION
Route Name ORAL
Start Marketing Date 20070601
Marketing Category Name ANDA
Labeler Name LUPIN PHARMA
Substance Name CEFIXIME
Strength Number 200
Strength Unit mg/5mL
Pharmaceutical Classes Cephalosporin Antibacterial [EPC],Cephalosporins [Chemical/Ingredient]

Complete Information of SUPRAX


General Information