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Gentamicin Sulfate in Sodium Chloride
Gentamicin Sulfate in Sodium Chloride - 0409-7889-23 - (GENTAMICIN SULFATE)
Drug Information of Gentamicin Sulfate in Sodium Chloride
| Product NDC: | 0409-7889 |
| Proprietary Name: | Gentamicin Sulfate in Sodium Chloride |
| Non Proprietary Name: | GENTAMICIN SULFATE |
| Active Ingredient(s): | 1 mg/mL & nbsp; GENTAMICIN SULFATE |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | INJECTION, SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Gentamicin Sulfate in Sodium Chloride
| Product NDC: | 0409-7889 |
| Labeler Name: | Hospira, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA062414 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20091204 |
Package Information of Gentamicin Sulfate in Sodium Chloride
| Package NDC: | 0409-7889-23 |
| Package Description: | 24 POUCH in 1 CASE (0409-7889-23) > 1 BAG in 1 POUCH > 100 mL in 1 BAG |
NDC Information of Gentamicin Sulfate in Sodium Chloride
| NDC Code | 0409-7889-23 |
| Proprietary Name | Gentamicin Sulfate in Sodium Chloride |
| Package Description | 24 POUCH in 1 CASE (0409-7889-23) > 1 BAG in 1 POUCH > 100 mL in 1 BAG |
| Product NDC | 0409-7889 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | GENTAMICIN SULFATE |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 20091204 |
| Marketing Category Name | ANDA |
| Labeler Name | Hospira, Inc. |
| Substance Name | GENTAMICIN SULFATE |
| Strength Number | 1 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Aminoglycoside Antibacterial [EPC],Aminoglycosides [Chemical/Ingredient] |
