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Cefditoren Pivoxil - 44009-801-20 - (cefditoren pivoxil)

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Drug Information of Cefditoren Pivoxil

Product NDC: 44009-801
Proprietary Name: Cefditoren Pivoxil
Non Proprietary Name: cefditoren pivoxil
Active Ingredient(s): 200    mg/1 & nbsp;   cefditoren pivoxil
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Cefditoren Pivoxil

Product NDC: 44009-801
Labeler Name: Pharma RomLev Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021222
Marketing Category: NDA
Start Marketing Date: 20130212

Package Information of Cefditoren Pivoxil

Package NDC: 44009-801-20
Package Description: 20 TABLET, FILM COATED in 1 BLISTER PACK (44009-801-20)

NDC Information of Cefditoren Pivoxil

NDC Code 44009-801-20
Proprietary Name Cefditoren Pivoxil
Package Description 20 TABLET, FILM COATED in 1 BLISTER PACK (44009-801-20)
Product NDC 44009-801
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name cefditoren pivoxil
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20130212
Marketing Category Name NDA
Labeler Name Pharma RomLev Inc.
Substance Name CEFDITOREN PIVOXIL
Strength Number 200
Strength Unit mg/1
Pharmaceutical Classes Cephalosporin Antibacterial [EPC],Cephalosporins [Chemical/Ingredient]

Complete Information of Cefditoren Pivoxil


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