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NDC 36000-0242-01 Tobramycin 40 mg/mL Details
Tobramycin 40 mg/mL
Tobramycin is a INTRAMUSCULAR; INTRAVENOUS INJECTION in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Baxter Healthcare Corporation. The primary component is TOBRAMYCIN SULFATE.
MedlinePlus Drug Summary
Tobramycin injection is used to treat certain serious infections that are caused by bacteria such as meningitis (infection of the membranes that surround the brain and spinal cord) and infections of the blood, abdomen (stomach area), lungs, skin, bones, joints, and urinary tract. Tobramycin injection is in a class of medications called aminoglycoside antibiotics. It works by killing bacteria. Antibiotics such as tobramycin injection will not work for colds, flu, or other viral infections. Taking antibiotics when they are not needed increases your risk of getting an infection later that resists antibiotic treatment.
Related Packages: 36000-0242-01Last Updated: 11/30/2022
MedLinePlus Full Drug Details: Tobramycin Injection
Product Information
| NDC | 36000-0242 |
|---|---|
| Product ID | 36000-242_48455a2b-67f2-431b-8931-0f9f3ec46286 |
| Associated GPIs | 07000070102038 |
| GCN Sequence Number | 009310 |
| GCN Sequence Number Description | tobramycin sulfate VIAL 40 MG/ML INJECTION |
| HIC3 | W1F |
| HIC3 Description | AMINOGLYCOSIDE ANTIBIOTICS |
| GCN | 41185 |
| HICL Sequence Number | 004034 |
| HICL Sequence Number Description | TOBRAMYCIN SULFATE |
| Brand/Generic | Generic |
| Proprietary Name | Tobramycin |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | Tobramycin |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Dosage Form | INJECTION |
| Route | INTRAMUSCULAR; INTRAVENOUS |
| Active Ingredient Strength | 40 |
| Active Ingredient Units | mg/mL |
| Substance Name | TOBRAMYCIN SULFATE |
| Labeler Name | Baxter Healthcare Corporation |
| Pharmaceutical Class | Aminoglycoside Antibacterial [EPC], Aminoglycosides [CS] |
| DEA Schedule | n/a |
| Marketing Category | ANDA |
| Application Number | ANDA206965 |
| Listing Certified Through | 2024-12-31 |
Package
NDC 36000-0242-01 (36000024201)
| NDC Package Code | 36000-242-01 |
|---|---|
| Billing NDC | 36000024201 |
| Package | 1 VIAL, MULTI-DOSE in 1 CARTON (36000-242-01) / 30 mL in 1 VIAL, MULTI-DOSE |
| Marketing Start Date | 2016-07-15 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |