Product NDC: | 54868-1040 |
Proprietary Name: | Gentamicin Sulfate |
Non Proprietary Name: | gentamicin sulfate |
Active Ingredient(s): | 3 mg/g & nbsp; gentamicin sulfate |
Administration Route(s): | OPHTHALMIC |
Dosage Form(s): | OINTMENT |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 54868-1040 |
Labeler Name: | Physicians Total Care, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA065024 |
Marketing Category: | ANDA |
Start Marketing Date: | 19940921 |
Package NDC: | 54868-1040-1 |
Package Description: | 3.5 g in 1 TUBE (54868-1040-1) |
NDC Code | 54868-1040-1 |
Proprietary Name | Gentamicin Sulfate |
Package Description | 3.5 g in 1 TUBE (54868-1040-1) |
Product NDC | 54868-1040 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | gentamicin sulfate |
Dosage Form Name | OINTMENT |
Route Name | OPHTHALMIC |
Start Marketing Date | 19940921 |
Marketing Category Name | ANDA |
Labeler Name | Physicians Total Care, Inc. |
Substance Name | GENTAMICIN SULFATE |
Strength Number | 3 |
Strength Unit | mg/g |
Pharmaceutical Classes | Aminoglycoside Antibacterial [EPC],Aminoglycosides [Chemical/Ingredient] |