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Tobramycin
Tobramycin - 39822-0412-6 - (Tobramycin)
Drug Information of Tobramycin
| Product NDC: | 39822-0412 |
| Proprietary Name: | Tobramycin |
| Non Proprietary Name: | Tobramycin |
| Active Ingredient(s): | 1.2 g/30mL & nbsp; Tobramycin |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Tobramycin
| Product NDC: | 39822-0412 |
| Labeler Name: | X-GEN Pharmaceuticals, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA065013 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20010817 |
Package Information of Tobramycin
| Package NDC: | 39822-0412-6 |
| Package Description: | 6 VIAL in 1 CARTON (39822-0412-6) > 30 mL in 1 VIAL |
NDC Information of Tobramycin
| NDC Code | 39822-0412-6 |
| Proprietary Name | Tobramycin |
| Package Description | 6 VIAL in 1 CARTON (39822-0412-6) > 30 mL in 1 VIAL |
| Product NDC | 39822-0412 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Tobramycin |
| Dosage Form Name | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 20010817 |
| Marketing Category Name | ANDA |
| Labeler Name | X-GEN Pharmaceuticals, Inc. |
| Substance Name | TOBRAMYCIN SULFATE |
| Strength Number | 1.2 |
| Strength Unit | g/30mL |
| Pharmaceutical Classes | Aminoglycoside Antibacterial [EPC],Aminoglycosides [Chemical/Ingredient] |
