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Cefpodoxime Proxetil
Cefpodoxime Proxetil - 0781-6169-52 - (Cefpodoxime Proxetil)
Drug Information of Cefpodoxime Proxetil
| Product NDC: | 0781-6169 |
| Proprietary Name: | Cefpodoxime Proxetil |
| Non Proprietary Name: | Cefpodoxime Proxetil |
| Active Ingredient(s): | 100 mg/5mL & nbsp; Cefpodoxime Proxetil |
| Administration Route(s): | ORAL |
| Dosage Form(s): | GRANULE, FOR SUSPENSION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Cefpodoxime Proxetil
| Product NDC: | 0781-6169 |
| Labeler Name: | Sandoz Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA090031 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20090625 |
Package Information of Cefpodoxime Proxetil
| Package NDC: | 0781-6169-52 |
| Package Description: | 1 BOTTLE in 1 CARTON (0781-6169-52) > 50 mL in 1 BOTTLE |
NDC Information of Cefpodoxime Proxetil
| NDC Code | 0781-6169-52 |
| Proprietary Name | Cefpodoxime Proxetil |
| Package Description | 1 BOTTLE in 1 CARTON (0781-6169-52) > 50 mL in 1 BOTTLE |
| Product NDC | 0781-6169 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Cefpodoxime Proxetil |
| Dosage Form Name | GRANULE, FOR SUSPENSION |
| Route Name | ORAL |
| Start Marketing Date | 20090625 |
| Marketing Category Name | ANDA |
| Labeler Name | Sandoz Inc |
| Substance Name | CEFPODOXIME PROXETIL |
| Strength Number | 100 |
| Strength Unit | mg/5mL |
| Pharmaceutical Classes | Cephalosporin Antibacterial [EPC],Cephalosporins [Chemical/Ingredient] |
