Product NDC: | 21695-204 |
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: | 21695-204 |
Labeler Name: | Rebel Distributors Corp |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA063176 |
Marketing Category: | ANDA |
Start Marketing Date: | 19940525 |
Package NDC: | 21695-204-05 |
Package Description: | 5 mL in 1 BOTTLE, PLASTIC (21695-204-05) |
NDC Code | 21695-204-05 |
Proprietary Name | Tobramycin |
Package Description | 5 mL in 1 BOTTLE, PLASTIC (21695-204-05) |
Product NDC | 21695-204 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | tobramycin |
Dosage Form Name | SOLUTION |
Route Name | OPHTHALMIC |
Start Marketing Date | 19940525 |
Marketing Category Name | ANDA |
Labeler Name | Rebel Distributors Corp |
Substance Name | TOBRAMYCIN |
Strength Number | 3 |
Strength Unit | mg/mL |
Pharmaceutical Classes | Aminoglycoside Antibacterial [EPC],Aminoglycosides [Chemical/Ingredient] |