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MAXIPIME
MAXIPIME - 55154-1056-5 - (CEFEPIME HYDROCHLORIDE)
Drug Information of MAXIPIME
| Product NDC: | 55154-1056 |
| Proprietary Name: | MAXIPIME |
| Non Proprietary Name: | CEFEPIME HYDROCHLORIDE |
| Active Ingredient(s): | 1 g/1 & nbsp; CEFEPIME HYDROCHLORIDE |
| Administration Route(s): | INTRAMUSCULAR; INTRAVENOUS |
| Dosage Form(s): | INJECTION, POWDER, FOR SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of MAXIPIME
| Product NDC: | 55154-1056 |
| Labeler Name: | Cardinal Health |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA050679 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19960118 |
Package Information of MAXIPIME
| Package NDC: | 55154-1056-5 |
| Package Description: | 5 VIAL in 1 BAG (55154-1056-5) > 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL |
NDC Information of MAXIPIME
| NDC Code | 55154-1056-5 |
| Proprietary Name | MAXIPIME |
| Package Description | 5 VIAL in 1 BAG (55154-1056-5) > 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL |
| Product NDC | 55154-1056 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | CEFEPIME HYDROCHLORIDE |
| Dosage Form Name | INJECTION, POWDER, FOR SOLUTION |
| Route Name | INTRAMUSCULAR; INTRAVENOUS |
| Start Marketing Date | 19960118 |
| Marketing Category Name | NDA |
| Labeler Name | Cardinal Health |
| Substance Name | CEFEPIME HYDROCHLORIDE |
| Strength Number | 1 |
| Strength Unit | g/1 |
| Pharmaceutical Classes | Cephalosporin Antibacterial [EPC],Cephalosporins [Chemical/Ingredient] |
