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
- 36000-244_19ade85b-3da4-44af-8ad0-d68d15a48193
- Product NDC
- 36000-244
- Form
- INJECTION
- Composition / generic term
- Tobramycin
- Labeler
- Baxter Healthcare Corporation
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20160715
- Source listing expiry
- 20261231
Source-listed ingredients
- TOBRAMYCIN SULFATE — 40 mg/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 25 VIAL, MULTI-DOSE in 1 BLISTER PACK (36000-244-25) / 2 mL in 1 VIAL, MULTI-DOSE · 36000-244-25
Source and coverage
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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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