United States · FDA National Drug Code directory
Gentamicin Sulfate in Sodium Chloride
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
- 0338-0509_aacff3ac-5df9-4872-b074-78930c9c9b79
- Product NDC
- 0338-0509
- Form
- INJECTION, SOLUTION
- Composition / generic term
- Gentamicin Sulfate
- Labeler
- Baxter Healthcare Corporation
- Marketing category
- ANDA
- Marketing start / end (source format)
- 19820907
- Source listing expiry
- 20271231
Source-listed ingredients
- GENTAMICIN SULFATE — 80 mg/50mL
These values do not establish equivalence or a dose recommendation.
Packages
- 50 mL in 1 BAG (0338-0509-41) · 0338-0509-41
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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