tobramycin
Generic: tobramycin
Labeler: baxter healthcare corporationDrug Facts
Product Profile
Brand Name
tobramycin
Generic Name
tobramycin
Labeler
baxter healthcare corporation
Dosage Form
INJECTION
Routes
Active Ingredients
tobramycin sulfate 40 mg/mL
Manufacturer
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
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
36000242
Hyphenated Format
36000-242
Supplemental Identifiers
RxCUI
UPC
UNII
Packaging Origin
Original Packager
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
source: ndc
Resolved Composition
Strengths
- 40 mg/mL
Packaging
- 1 VIAL, MULTI-DOSE in 1 CARTON (36000-242-01) / 30 mL in 1 VIAL, MULTI-DOSE
Packages (1)
Ingredients (1)
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"}