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Cefpodoxime Proxetil
Cefpodoxime Proxetil - 0781-5439-20 - (Cefpodoxime Proxetil)
Drug Information of Cefpodoxime Proxetil
| Product NDC: | 0781-5439 |
| Proprietary Name: | Cefpodoxime Proxetil |
| Non Proprietary Name: | Cefpodoxime Proxetil |
| Active Ingredient(s): | 200 mg/1 & nbsp; Cefpodoxime Proxetil |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Cefpodoxime Proxetil
| Product NDC: | 0781-5439 |
| Labeler Name: | Sandoz Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA065462 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20080528 |
Package Information of Cefpodoxime Proxetil
| Package NDC: | 0781-5439-20 |
| Package Description: | 20 TABLET, FILM COATED in 1 BOTTLE (0781-5439-20) |
NDC Information of Cefpodoxime Proxetil
| NDC Code | 0781-5439-20 |
| Proprietary Name | Cefpodoxime Proxetil |
| Package Description | 20 TABLET, FILM COATED in 1 BOTTLE (0781-5439-20) |
| Product NDC | 0781-5439 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Cefpodoxime Proxetil |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20080528 |
| Marketing Category Name | ANDA |
| Labeler Name | Sandoz Inc |
| Substance Name | CEFPODOXIME PROXETIL |
| Strength Number | 200 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Cephalosporin Antibacterial [EPC],Cephalosporins [Chemical/Ingredient] |
