Product NDC: | 63323-173 |
Proprietary Name: | Gentamicin |
Non Proprietary Name: | GENTAMICIN |
Active Ingredient(s): | 10 mg/mL & nbsp; GENTAMICIN |
Administration Route(s): | INTRAMUSCULAR; INTRAVENOUS |
Dosage Form(s): | INJECTION, SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 63323-173 |
Labeler Name: | APP Pharmaceuticals, LLC |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA062366 |
Marketing Category: | ANDA |
Start Marketing Date: | 20041129 |
Package NDC: | 63323-173-02 |
Package Description: | 25 VIAL in 1 TRAY (63323-173-02) > 2 mL in 1 VIAL |
NDC Code | 63323-173-02 |
Proprietary Name | Gentamicin |
Package Description | 25 VIAL in 1 TRAY (63323-173-02) > 2 mL in 1 VIAL |
Product NDC | 63323-173 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | GENTAMICIN |
Dosage Form Name | INJECTION, SOLUTION |
Route Name | INTRAMUSCULAR; INTRAVENOUS |
Start Marketing Date | 20041129 |
Marketing Category Name | ANDA |
Labeler Name | APP Pharmaceuticals, LLC |
Substance Name | GENTAMICIN SULFATE |
Strength Number | 10 |
Strength Unit | mg/mL |
Pharmaceutical Classes | Aminoglycoside Antibacterial [EPC],Aminoglycosides [Chemical/Ingredient] |