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CEFTIN
CEFTIN - 0173-0741-00 - (cefuroxime axetil)
Drug Information of CEFTIN
| Product NDC: | 0173-0741 |
| Proprietary Name: | CEFTIN |
| Non Proprietary Name: | cefuroxime axetil |
| Active Ingredient(s): | 250 mg/5mL & nbsp; cefuroxime axetil |
| Administration Route(s): | ORAL |
| Dosage Form(s): | POWDER, FOR SUSPENSION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of CEFTIN
| Product NDC: | 0173-0741 |
| Labeler Name: | GlaxoSmithKline LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA050672 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20040602 |
Package Information of CEFTIN
| Package NDC: | 0173-0741-00 |
| Package Description: | 100 mL in 1 BOTTLE, GLASS (0173-0741-00) |
NDC Information of CEFTIN
| NDC Code | 0173-0741-00 |
| Proprietary Name | CEFTIN |
| Package Description | 100 mL in 1 BOTTLE, GLASS (0173-0741-00) |
| Product NDC | 0173-0741 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | cefuroxime axetil |
| Dosage Form Name | POWDER, FOR SUSPENSION |
| Route Name | ORAL |
| Start Marketing Date | 20040602 |
| Marketing Category Name | NDA |
| Labeler Name | GlaxoSmithKline LLC |
| Substance Name | CEFUROXIME AXETIL |
| Strength Number | 250 |
| Strength Unit | mg/5mL |
| Pharmaceutical Classes | Cephalosporin Antibacterial [EPC],Cephalosporins [Chemical/Ingredient] |
