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Vantin
Vantin - 55289-390-79 - (cefpodoxime proxetil)
Drug Information of Vantin
| Product NDC: | 55289-390 |
| Proprietary Name: | Vantin |
| 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 Vantin
| Product NDC: | 55289-390 |
| Labeler Name: | PD-Rx Pharmaceuticals, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA050674 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19910829 |
Package Information of Vantin
| Package NDC: | 55289-390-79 |
| Package Description: | 1 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (55289-390-79) |
NDC Information of Vantin
| NDC Code | 55289-390-79 |
| Proprietary Name | Vantin |
| Package Description | 1 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (55289-390-79) |
| Product NDC | 55289-390 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | cefpodoxime proxetil |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 19910829 |
| Marketing Category Name | NDA |
| Labeler Name | PD-Rx Pharmaceuticals, Inc. |
| Substance Name | CEFPODOXIME PROXETIL |
| Strength Number | 200 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Cephalosporin Antibacterial [EPC],Cephalosporins [Chemical/Ingredient] |
