United States · FDA National Drug Code directory

Tobramycin

A source-listed medicine record.

Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.

Medicine identity

Source reference
63323-303_ea244093-d87f-4192-b5c4-59d7b7dbf669
Product NDC
63323-303
Form
INJECTION, POWDER, FOR SOLUTION
Composition / generic term
TOBRAMYCIN SULFATE
Labeler
Fresenius Kabi USA, LLC
Marketing category
NDA
Marketing start / end (source format)
20051123
Source listing expiry
20261231

Source-listed ingredients

  • TOBRAMYCIN SULFATE — 1200 mg/30mL

These values do not establish equivalence or a dose recommendation.

Packages

  • 6 VIAL, PHARMACY BULK PACKAGE in 1 TRAY (63323-303-51) / 30 mL in 1 VIAL, PHARMACY BULK PACKAGE (63323-303-01) · 63323-303-51

Source and coverage

Open FDA National Drug Code directory

Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.

Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.

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Tobramycin — United States | Molindra Medicines