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Cefuroxime Axetil
Cefuroxime Axetil - 52959-939-20 - (Cefuroxime Axetil)
Drug Information of Cefuroxime Axetil
| Product NDC: | 52959-939 |
| Proprietary Name: | Cefuroxime Axetil |
| Non Proprietary Name: | Cefuroxime Axetil |
| Active Ingredient(s): | 500 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: | 52959-939 |
| Labeler Name: | H.J. Harkins Company, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA065308 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20060329 |
Package Information of Cefuroxime Axetil
| Package NDC: | 52959-939-20 |
| Package Description: | 20 TABLET in 1 BOTTLE (52959-939-20) |
NDC Information of Cefuroxime Axetil
| NDC Code | 52959-939-20 |
| Proprietary Name | Cefuroxime Axetil |
| Package Description | 20 TABLET in 1 BOTTLE (52959-939-20) |
| Product NDC | 52959-939 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Cefuroxime Axetil |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20060329 |
| Marketing Category Name | ANDA |
| Labeler Name | H.J. Harkins Company, Inc. |
| Substance Name | CEFUROXIME AXETIL |
| Strength Number | 500 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Cephalosporin Antibacterial [EPC],Cephalosporins [Chemical/Ingredient] |
