United States · FDA National Drug Code directory
Amikacin Sulfate
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
- 23155-785_7f946330-e4c6-4643-903d-3695d08df7d6
- Product NDC
- 23155-785
- Form
- INJECTION, SOLUTION
- Composition / generic term
- Amikacin Sulfate
- Labeler
- Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20201215
- Source listing expiry
- 20261231
Source-listed ingredients
- AMIKACIN SULFATE — 500 mg/2mL
These values do not establish equivalence or a dose recommendation.
Packages
- 10 VIAL, GLASS in 1 CARTON (23155-785-41) / 2 mL in 1 VIAL, GLASS (23155-785-31) · 23155-785-41
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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