SUPRAX - 27437-203-10 - (cefixime)

Alphabetical Index


Drug Information of SUPRAX

Product NDC: 27437-203
Proprietary Name: SUPRAX
Non Proprietary Name: cefixime
Active Ingredient(s): 100    mg/1 & nbsp;   cefixime
Administration Route(s): ORAL
Dosage Form(s): TABLET, CHEWABLE
Coding System: National Drug Codes(NDC)

Labeler Information of SUPRAX

Product NDC: 27437-203
Labeler Name: LUPIN PHARMA
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA065380
Marketing Category: ANDA
Start Marketing Date: 20121205

Package Information of SUPRAX

Package NDC: 27437-203-10
Package Description: 10 TABLET, CHEWABLE in 1 BOTTLE (27437-203-10)

NDC Information of SUPRAX

NDC Code 27437-203-10
Proprietary Name SUPRAX
Package Description 10 TABLET, CHEWABLE in 1 BOTTLE (27437-203-10)
Product NDC 27437-203
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name cefixime
Dosage Form Name TABLET, CHEWABLE
Route Name ORAL
Start Marketing Date 20121205
Marketing Category Name ANDA
Labeler Name LUPIN PHARMA
Substance Name CEFIXIME
Strength Number 100
Strength Unit mg/1
Pharmaceutical Classes Cephalosporin Antibacterial [EPC],Cephalosporins [Chemical/Ingredient]

Complete Information of SUPRAX


General Information