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cefuroxime axetil
cefuroxime axetil - 68788-9700-6 - (cefuroxime axetil)
Drug Information of cefuroxime axetil
| Product NDC: | 68788-9700 |
| Proprietary Name: | cefuroxime axetil |
| Non Proprietary Name: | cefuroxime axetil |
| Active Ingredient(s): | 250 mg/1 & nbsp; cefuroxime axetil |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of cefuroxime axetil
| Product NDC: | 68788-9700 |
| Labeler Name: | Preferred Pharmaceuticals, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA065135 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20130315 |
Package Information of cefuroxime axetil
| Package NDC: | 68788-9700-6 |
| Package Description: | 60 TABLET in 1 BOTTLE (68788-9700-6) |
NDC Information of cefuroxime axetil
| NDC Code | 68788-9700-6 |
| Proprietary Name | cefuroxime axetil |
| Package Description | 60 TABLET in 1 BOTTLE (68788-9700-6) |
| Product NDC | 68788-9700 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | cefuroxime axetil |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20130315 |
| Marketing Category Name | ANDA |
| Labeler Name | Preferred Pharmaceuticals, Inc. |
| Substance Name | CEFUROXIME AXETIL |
| Strength Number | 250 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Cephalosporin Antibacterial [EPC],Cephalosporins [Chemical/Ingredient] |
