tobramycin

Generic: tobramycin

Labeler: baxter healthcare corporation
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name tobramycin
Generic Name tobramycin
Labeler baxter healthcare corporation
Dosage Form INJECTION
Routes
INTRAMUSCULAR INTRAVENOUS
Active Ingredients

tobramycin sulfate 40 mg/mL

Manufacturer
Baxter Healthcare Corporation

Identifiers & Regulatory

Product NDC 36000-242
Product ID 36000-242_19ade85b-3da4-44af-8ad0-d68d15a48193
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA206965
Listing Expiration 2026-12-31
Marketing Start 2016-07-15

Pharmacologic Class

Classes
aminoglycoside antibacterial [epc] aminoglycosides [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 36000242
Hyphenated Format 36000-242

Supplemental Identifiers

RxCUI
597823
UPC
0336000244015 0336000242011
UNII
HJT0RXD7JK

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name tobramycin (source: ndc)
Generic Name tobramycin (source: ndc)
Application Number ANDA206965 (source: ndc)
Routes
INTRAMUSCULAR INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 40 mg/mL
source: ndc
Packaging
  • 1 VIAL, MULTI-DOSE in 1 CARTON (36000-242-01) / 30 mL in 1 VIAL, MULTI-DOSE
source: ndc

Packages (1)

Ingredients (1)

tobramycin sulfate (40 mg/mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "19ade85b-3da4-44af-8ad0-d68d15a48193", "openfda": {"upc": ["0336000244015", "0336000242011"], "unii": ["HJT0RXD7JK"], "rxcui": ["597823"], "spl_set_id": ["a9897444-71f6-42af-9b71-4aa77829ade0"], "manufacturer_name": ["Baxter Healthcare Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, MULTI-DOSE in 1 CARTON (36000-242-01)  / 30 mL in 1 VIAL, MULTI-DOSE", "package_ndc": "36000-242-01", "marketing_start_date": "20160715"}], "brand_name": "Tobramycin", "product_id": "36000-242_19ade85b-3da4-44af-8ad0-d68d15a48193", "dosage_form": "INJECTION", "pharm_class": ["Aminoglycoside Antibacterial [EPC]", "Aminoglycosides [CS]"], "product_ndc": "36000-242", "generic_name": "Tobramycin", "labeler_name": "Baxter Healthcare Corporation", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Tobramycin", "active_ingredients": [{"name": "TOBRAMYCIN SULFATE", "strength": "40 mg/mL"}], "application_number": "ANDA206965", "marketing_category": "ANDA", "marketing_start_date": "20160715", "listing_expiration_date": "20261231"}