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Cefuroxime
Cefuroxime - 63323-352-45 - (Cefuroxime)
Drug Information of Cefuroxime
| Product NDC: | 63323-352 |
| Proprietary Name: | Cefuroxime |
| Non Proprietary Name: | Cefuroxime |
| Active Ingredient(s): | 750 mg/1 & nbsp; Cefuroxime |
| Administration Route(s): | INTRAMUSCULAR; INTRAVENOUS |
| Dosage Form(s): | INJECTION, POWDER, FOR SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Cefuroxime
| Product NDC: | 63323-352 |
| Labeler Name: | APP Pharmaceuticals, LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA064125 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20110524 |
Package Information of Cefuroxime
| Package NDC: | 63323-352-45 |
| Package Description: | 25 INJECTION, POWDER, FOR SOLUTION in 1 CARTON (63323-352-45) |
NDC Information of Cefuroxime
| NDC Code | 63323-352-45 |
| Proprietary Name | Cefuroxime |
| Package Description | 25 INJECTION, POWDER, FOR SOLUTION in 1 CARTON (63323-352-45) |
| Product NDC | 63323-352 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Cefuroxime |
| Dosage Form Name | INJECTION, POWDER, FOR SOLUTION |
| Route Name | INTRAMUSCULAR; INTRAVENOUS |
| Start Marketing Date | 20110524 |
| Marketing Category Name | ANDA |
| Labeler Name | APP Pharmaceuticals, LLC |
| Substance Name | CEFUROXIME |
| Strength Number | 750 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Cephalosporin Antibacterial [EPC],Cephalosporins [Chemical/Ingredient] |
