Product NDC: | 61314-643 |
Proprietary Name: | Tobramycin |
Non Proprietary Name: | Tobramycin |
Active Ingredient(s): | 3 mg/mL & nbsp; Tobramycin |
Administration Route(s): | OPHTHALMIC |
Dosage Form(s): | SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 61314-643 |
Labeler Name: | Sandoz Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA062535 |
Marketing Category: | ANDA |
Start Marketing Date: | 19950109 |
Package NDC: | 61314-643-05 |
Package Description: | 5 mL in 1 BOTTLE, PLASTIC (61314-643-05) |
NDC Code | 61314-643-05 |
Proprietary Name | Tobramycin |
Package Description | 5 mL in 1 BOTTLE, PLASTIC (61314-643-05) |
Product NDC | 61314-643 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Tobramycin |
Dosage Form Name | SOLUTION |
Route Name | OPHTHALMIC |
Start Marketing Date | 19950109 |
Marketing Category Name | ANDA |
Labeler Name | Sandoz Inc. |
Substance Name | TOBRAMYCIN |
Strength Number | 3 |
Strength Unit | mg/mL |
Pharmaceutical Classes | Aminoglycoside Antibacterial [EPC],Aminoglycosides [Chemical/Ingredient] |