Product NDC: | 0904-2970 |
Proprietary Name: | Tobramycin |
Non Proprietary Name: | Tobramycin |
Active Ingredient(s): | 3 mg/mL & nbsp; Tobramycin |
Administration Route(s): | OPHTHALMIC |
Dosage Form(s): | SOLUTION/ DROPS |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0904-2970 |
Labeler Name: | Major Pharmaceuticals |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA064052 |
Marketing Category: | ANDA |
Start Marketing Date: | 19931129 |
Package NDC: | 0904-2970-05 |
Package Description: | 1 BOTTLE, DROPPER in 1 CARTON (0904-2970-05) > 5 mL in 1 BOTTLE, DROPPER |
NDC Code | 0904-2970-05 |
Proprietary Name | Tobramycin |
Package Description | 1 BOTTLE, DROPPER in 1 CARTON (0904-2970-05) > 5 mL in 1 BOTTLE, DROPPER |
Product NDC | 0904-2970 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Tobramycin |
Dosage Form Name | SOLUTION/ DROPS |
Route Name | OPHTHALMIC |
Start Marketing Date | 19931129 |
Marketing Category Name | ANDA |
Labeler Name | Major Pharmaceuticals |
Substance Name | TOBRAMYCIN |
Strength Number | 3 |
Strength Unit | mg/mL |
Pharmaceutical Classes | Aminoglycoside Antibacterial [EPC],Aminoglycosides [Chemical/Ingredient] |