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Cefuroxime axetil
Cefuroxime axetil - 67877-215-20 - (Cefuroxime axetil)
Drug Information of Cefuroxime axetil
| Product NDC: | 67877-215 |
| 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, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Cefuroxime axetil
| Product NDC: | 67877-215 |
| Labeler Name: | Ascend Laboratories, LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA065496 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20101201 |
Package Information of Cefuroxime axetil
| Package NDC: | 67877-215-20 |
| Package Description: | 20 TABLET, FILM COATED in 1 BOTTLE (67877-215-20) |
NDC Information of Cefuroxime axetil
| NDC Code | 67877-215-20 |
| Proprietary Name | Cefuroxime axetil |
| Package Description | 20 TABLET, FILM COATED in 1 BOTTLE (67877-215-20) |
| Product NDC | 67877-215 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Cefuroxime axetil |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20101201 |
| Marketing Category Name | ANDA |
| Labeler Name | Ascend Laboratories, LLC |
| Substance Name | CEFUROXIME AXETIL |
| Strength Number | 250 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Cephalosporin Antibacterial [EPC],Cephalosporins [Chemical/Ingredient] |
