United States · FDA National Drug Code directory
Neomycin and Polymyxin B Sulfates and Hydrocortisone
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
- 61314-641_15cc1b8f-5a7f-4cfb-8c65-9d35f7c0f30f
- Product NDC
- 61314-641
- Form
- SUSPENSION
- Composition / generic term
- neomycin sulfate, polymyxin b sulfate and hydrocortisone
- Labeler
- Sandoz Inc
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20030509
- Source listing expiry
- 20261231
Source-listed ingredients
- NEOMYCIN SULFATE — 3.5 mg/mL
- POLYMYXIN B SULFATE — 10000 [USP'U]/mL
- HYDROCORTISONE — 10 mg/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 7.5 mL in 1 BOTTLE, PLASTIC (61314-641-75) · 61314-641-75
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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