Product NDC: | 0409-1207 |
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) |
Product NDC: | 0409-1207 |
Labeler Name: | Hospira, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA062420 |
Marketing Category: | ANDA |
Start Marketing Date: | 20110510 |
Package NDC: | 0409-1207-03 |
Package Description: | 25 VIAL, SINGLE-DOSE in 1 TRAY (0409-1207-03) > 2 mL in 1 VIAL, SINGLE-DOSE |
NDC Code | 0409-1207-03 |
Proprietary Name | Gentamicin Sulfate |
Package Description | 25 VIAL, SINGLE-DOSE in 1 TRAY (0409-1207-03) > 2 mL in 1 VIAL, SINGLE-DOSE |
Product NDC | 0409-1207 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | GENTAMICIN SULFATE |
Dosage Form Name | INJECTION, SOLUTION, CONCENTRATE |
Route Name | INTRAMUSCULAR; INTRAVENOUS |
Start Marketing Date | 20110510 |
Marketing Category Name | ANDA |
Labeler Name | Hospira, Inc. |
Substance Name | GENTAMICIN SULFATE |
Strength Number | 40 |
Strength Unit | mg/mL |
Pharmaceutical Classes | Aminoglycoside Antibacterial [EPC],Aminoglycosides [Chemical/Ingredient] |