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
- 39822-0412_40a90656-9bc2-494b-e063-6294a90a04f2
- Product NDC
- 39822-0412
- Form
- INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
- Composition / generic term
- Tobramycin
- Labeler
- XGen Pharmaceuticals DJB, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20010817
- Source listing expiry
- 20271231
Source-listed ingredients
- TOBRAMYCIN SULFATE — 1.2 g/30mL
These values do not establish equivalence or a dose recommendation.
Packages
- 1 VIAL in 1 CARTON (39822-0412-1) / 30 mL in 1 VIAL · 39822-0412-1
- 6 VIAL in 1 CARTON (39822-0412-6) / 30 mL in 1 VIAL · 39822-0412-6
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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