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
50090-0431_29d9c79c-f605-4755-996a-7dc78ecb89e7
Product NDC
50090-0431
Form
SUSPENSION/ DROPS
Composition / generic term
Neomycin sulfate, Polymyxin B Sulfate and Hydrocortisone
Labeler
A-S Medication Solutions
Marketing category
ANDA
Marketing start / end (source format)
19960828
Source listing expiry
20271231

Source-listed ingredients

  • HYDROCORTISONE — 10 mg/mL
  • NEOMYCIN SULFATE — 3.5 mg/mL
  • POLYMYXIN B SULFATE — 10000 [USP'U]/mL

These values do not establish equivalence or a dose recommendation.

Packages

  • 1 BOTTLE, DROPPER in 1 CARTON (50090-0431-0) / 10 mL in 1 BOTTLE, DROPPER · 50090-0431-0

Source and coverage

Open FDA National Drug Code directory

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.

Browse United States records →