Product NDC: | 44004-801 |
Proprietary Name: | Spectracef |
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) |
Product NDC: | 44004-801 |
Labeler Name: | Vansen Pharma Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA021222 |
Marketing Category: | NDA |
Start Marketing Date: | 20130205 |
Package NDC: | 44004-801-20 |
Package Description: | 20 TABLET, FILM COATED in 1 BLISTER PACK (44004-801-20) |
NDC Code | 44004-801-20 |
Proprietary Name | Spectracef |
Package Description | 20 TABLET, FILM COATED in 1 BLISTER PACK (44004-801-20) |
Product NDC | 44004-801 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | cefditoren pivoxil |
Dosage Form Name | TABLET, FILM COATED |
Route Name | ORAL |
Start Marketing Date | 20130205 |
Marketing Category Name | NDA |
Labeler Name | Vansen Pharma Inc. |
Substance Name | CEFDITOREN PIVOXIL |
Strength Number | 200 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Cephalosporin Antibacterial [EPC],Cephalosporins [Chemical/Ingredient] |