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Gentamicin
Gentamicin - 55154-9552-5 - (GENTAMICIN SULFATE)
Drug Information of Gentamicin
| Product NDC: | 55154-9552 |
| Proprietary Name: | Gentamicin |
| Non Proprietary Name: | GENTAMICIN SULFATE |
| Active Ingredient(s): | 10 mg/mL & nbsp; GENTAMICIN SULFATE |
| Administration Route(s): | INTRAMUSCULAR; INTRAVENOUS |
| Dosage Form(s): | INJECTION, SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Gentamicin
| Product NDC: | 55154-9552 |
| Labeler Name: | Cardinal Health |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA062356 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19820304 |
Package Information of Gentamicin
| Package NDC: | 55154-9552-5 |
| Package Description: | 5 VIAL in 1 BAG (55154-9552-5) > 2 mL in 1 VIAL |
NDC Information of Gentamicin
| NDC Code | 55154-9552-5 |
| Proprietary Name | Gentamicin |
| Package Description | 5 VIAL in 1 BAG (55154-9552-5) > 2 mL in 1 VIAL |
| Product NDC | 55154-9552 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | GENTAMICIN SULFATE |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | INTRAMUSCULAR; INTRAVENOUS |
| Start Marketing Date | 19820304 |
| Marketing Category Name | ANDA |
| Labeler Name | Cardinal Health |
| Substance Name | GENTAMICIN SULFATE |
| Strength Number | 10 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Aminoglycoside Antibacterial [EPC],Aminoglycosides [Chemical/Ingredient] |
