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Cefepime
Cefepime - 63323-326-20 - (Cefepime)
Drug Information of Cefepime
| Product NDC: | 63323-326 |
| Proprietary Name: | Cefepime |
| Non Proprietary Name: | Cefepime |
| Active Ingredient(s): | 1 g/1 & nbsp; Cefepime |
| Administration Route(s): | INTRAMUSCULAR; INTRAVENOUS |
| Dosage Form(s): | INJECTION, POWDER, FOR SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Cefepime
| Product NDC: | 63323-326 |
| Labeler Name: | APP Pharmaceuticals, LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA065441 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20100830 |
Package Information of Cefepime
| Package NDC: | 63323-326-20 |
| Package Description: | 10 VIAL in 1 CARTON (63323-326-20) > 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL |
NDC Information of Cefepime
| NDC Code | 63323-326-20 |
| Proprietary Name | Cefepime |
| Package Description | 10 VIAL in 1 CARTON (63323-326-20) > 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL |
| Product NDC | 63323-326 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Cefepime |
| Dosage Form Name | INJECTION, POWDER, FOR SOLUTION |
| Route Name | INTRAMUSCULAR; INTRAVENOUS |
| Start Marketing Date | 20100830 |
| Marketing Category Name | ANDA |
| Labeler Name | APP Pharmaceuticals, LLC |
| Substance Name | CEFEPIME HYDROCHLORIDE |
| Strength Number | 1 |
| Strength Unit | g/1 |
| Pharmaceutical Classes | Cephalosporin Antibacterial [EPC],Cephalosporins [Chemical/Ingredient] |
