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
63323-305_c55fcee9-70c7-4926-bee6-014c0b133249
Product NDC
63323-305
Form
INJECTION, SOLUTION
Composition / generic term
TOBRAMYCIN SULFATE
Labeler
Fresenius Kabi USA, LLC
Marketing category
ANDA
Marketing start / end (source format)
20041130
Source listing expiry
20261231

Source-listed ingredients

  • TOBRAMYCIN SULFATE — 10 mg/mL

These values do not establish equivalence or a dose recommendation.

Packages

  • 25 VIAL, MULTI-DOSE in 1 TRAY (63323-305-02) / 2 mL in 1 VIAL, MULTI-DOSE (63323-305-01) · 63323-305-02

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