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Gentamicin Sulfate
Gentamicin Sulfate - 55154-2392-8 - (Gentamicin Sulfate)
Drug Information of Gentamicin Sulfate
| Product NDC: | 55154-2392 |
| Proprietary Name: | Gentamicin Sulfate |
| Non Proprietary Name: | Gentamicin Sulfate |
| Active Ingredient(s): | 40 mg/mL & nbsp; Gentamicin Sulfate |
| Administration Route(s): | INTRAMUSCULAR; INTRAVENOUS |
| Dosage Form(s): | INJECTION, SOLUTION, CONCENTRATE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Gentamicin Sulfate
| Product NDC: | 55154-2392 |
| Labeler Name: | Cardinal Health |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA062420 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19830815 |
Package Information of Gentamicin Sulfate
| Package NDC: | 55154-2392-8 |
| Package Description: | 1 VIAL, SINGLE-DOSE in 1 BAG (55154-2392-8) > 2 mL in 1 VIAL, SINGLE-DOSE |
NDC Information of Gentamicin Sulfate
| NDC Code | 55154-2392-8 |
| Proprietary Name | Gentamicin Sulfate |
| Package Description | 1 VIAL, SINGLE-DOSE in 1 BAG (55154-2392-8) > 2 mL in 1 VIAL, SINGLE-DOSE |
| Product NDC | 55154-2392 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Gentamicin Sulfate |
| Dosage Form Name | INJECTION, SOLUTION, CONCENTRATE |
| Route Name | INTRAMUSCULAR; INTRAVENOUS |
| Start Marketing Date | 19830815 |
| Marketing Category Name | ANDA |
| Labeler Name | Cardinal Health |
| Substance Name | GENTAMICIN SULFATE |
| Strength Number | 40 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Aminoglycoside Antibacterial [EPC],Aminoglycosides [Chemical/Ingredient] |
