Product NDC: | 54569-1144 |
Proprietary Name: | Gentamicin sulfate |
Non Proprietary Name: | Gentamicin Sulfate |
Active Ingredient(s): | 1 mg/g & nbsp; Gentamicin Sulfate |
Administration Route(s): | TOPICAL |
Dosage Form(s): | OINTMENT |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 54569-1144 |
Labeler Name: | A-S Medication Solutions LLC |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA062533 |
Marketing Category: | ANDA |
Start Marketing Date: | 20100317 |
Package NDC: | 54569-1144-0 |
Package Description: | 15 g in 1 TUBE (54569-1144-0) |
NDC Code | 54569-1144-0 |
Proprietary Name | Gentamicin sulfate |
Package Description | 15 g in 1 TUBE (54569-1144-0) |
Product NDC | 54569-1144 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Gentamicin Sulfate |
Dosage Form Name | OINTMENT |
Route Name | TOPICAL |
Start Marketing Date | 20100317 |
Marketing Category Name | ANDA |
Labeler Name | A-S Medication Solutions LLC |
Substance Name | GENTAMICIN |
Strength Number | 1 |
Strength Unit | mg/g |
Pharmaceutical Classes | Aminoglycoside Antibacterial [EPC],Aminoglycosides [Chemical/Ingredient] |