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AMIKACIN Sulfate
AMIKACIN Sulfate - 0409-1956-01 - (AMIKACIN SULFATE)
Drug Information of AMIKACIN Sulfate
| Product NDC: | 0409-1956 |
| Proprietary Name: | AMIKACIN Sulfate |
| Non Proprietary Name: | AMIKACIN SULFATE |
| Active Ingredient(s): | 500 mg/2mL & nbsp; AMIKACIN SULFATE |
| Administration Route(s): | INTRAMUSCULAR; INTRAVENOUS |
| Dosage Form(s): | INJECTION, SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of AMIKACIN Sulfate
| Product NDC: | 0409-1956 |
| Labeler Name: | Hospira, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA063264 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20110708 |
Package Information of AMIKACIN Sulfate
| Package NDC: | 0409-1956-01 |
| Package Description: | 10 VIAL, SINGLE-DOSE in 1 CARTON (0409-1956-01) > 2 mL in 1 VIAL, SINGLE-DOSE |
NDC Information of AMIKACIN Sulfate
| NDC Code | 0409-1956-01 |
| Proprietary Name | AMIKACIN Sulfate |
| Package Description | 10 VIAL, SINGLE-DOSE in 1 CARTON (0409-1956-01) > 2 mL in 1 VIAL, SINGLE-DOSE |
| Product NDC | 0409-1956 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | AMIKACIN SULFATE |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | INTRAMUSCULAR; INTRAVENOUS |
| Start Marketing Date | 20110708 |
| Marketing Category Name | ANDA |
| Labeler Name | Hospira, Inc. |
| Substance Name | AMIKACIN SULFATE |
| Strength Number | 500 |
| Strength Unit | mg/2mL |
| Pharmaceutical Classes | Aminoglycoside Antibacterial [EPC],Aminoglycosides [Chemical/Ingredient] |
