tobramycin
Generic: tobramycin sulfate
Labeler: fresenius kabi usa, llcDrug Facts
Product Profile
Brand Name
tobramycin
Generic Name
tobramycin sulfate
Labeler
fresenius kabi usa, llc
Dosage Form
INJECTION, POWDER, FOR SOLUTION
Routes
Active Ingredients
tobramycin sulfate 1200 mg/30mL
Manufacturer
Identifiers & Regulatory
Product NDC
63323-303
Product ID
63323-303_ea244093-d87f-4192-b5c4-59d7b7dbf669
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
NDA
Application Number
NDA050789
Listing Expiration
2026-12-31
Marketing Start
2005-11-23
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
63323303
Hyphenated Format
63323-303
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 sulfate (source: ndc)
Application Number
NDA050789 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 1200 mg/30mL
Packaging
- 6 VIAL, PHARMACY BULK PACKAGE in 1 TRAY (63323-303-51) / 30 mL in 1 VIAL, PHARMACY BULK PACKAGE (63323-303-01)
Packages (1)
Ingredients (1)
Linked Drug Pages (2)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "ea244093-d87f-4192-b5c4-59d7b7dbf669", "openfda": {"upc": ["0363323303013"], "unii": ["HJT0RXD7JK"], "rxcui": ["597823"], "spl_set_id": ["d62ff359-912b-4be1-9fc2-2dde8777eefb"], "manufacturer_name": ["Fresenius Kabi USA, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "6 VIAL, PHARMACY BULK PACKAGE in 1 TRAY (63323-303-51) / 30 mL in 1 VIAL, PHARMACY BULK PACKAGE (63323-303-01)", "package_ndc": "63323-303-51", "marketing_start_date": "20051123"}], "brand_name": "Tobramycin", "product_id": "63323-303_ea244093-d87f-4192-b5c4-59d7b7dbf669", "dosage_form": "INJECTION, POWDER, FOR SOLUTION", "pharm_class": ["Aminoglycoside Antibacterial [EPC]", "Aminoglycosides [CS]"], "product_ndc": "63323-303", "generic_name": "TOBRAMYCIN SULFATE", "labeler_name": "Fresenius Kabi USA, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Tobramycin", "active_ingredients": [{"name": "TOBRAMYCIN SULFATE", "strength": "1200 mg/30mL"}], "application_number": "NDA050789", "marketing_category": "NDA", "marketing_start_date": "20051123", "listing_expiration_date": "20261231"}