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Gentamicin
Gentamicin - 63323-010-02 - (GENTAMICIN SULFATE)
Drug Information of Gentamicin
| Product NDC: | 63323-010 |
| Proprietary Name: | Gentamicin |
| Non Proprietary Name: | GENTAMICIN SULFATE |
| Active Ingredient(s): | 40 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: | 63323-010 |
| Labeler Name: | APP Pharmaceuticals, LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA062366 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20000810 |
Package Information of Gentamicin
| Package NDC: | 63323-010-02 |
| Package Description: | 25 VIAL, MULTI-DOSE in 1 TRAY (63323-010-02) > 2 mL in 1 VIAL, MULTI-DOSE |
NDC Information of Gentamicin
| NDC Code | 63323-010-02 |
| Proprietary Name | Gentamicin |
| Package Description | 25 VIAL, MULTI-DOSE in 1 TRAY (63323-010-02) > 2 mL in 1 VIAL, MULTI-DOSE |
| Product NDC | 63323-010 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | GENTAMICIN SULFATE |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | INTRAMUSCULAR; INTRAVENOUS |
| Start Marketing Date | 20000810 |
| Marketing Category Name | ANDA |
| Labeler Name | APP Pharmaceuticals, LLC |
| Substance Name | GENTAMICIN SULFATE |
| Strength Number | 40 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Aminoglycoside Antibacterial [EPC],Aminoglycosides [Chemical/Ingredient] |
