United States · FDA National Drug Code directory
MAXITROL
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
- 0078-0771_6328676b-98d9-4548-bc41-117e0e21eba6
- Product NDC
- 0078-0771
- Form
- OINTMENT
- Composition / generic term
- neomycin sulfate, polymyxin b sulfate and dexamethasone
- Labeler
- Novartis Pharmaceuticals Corporation
- Marketing category
- NDA
- Marketing start / end (source format)
- 19720117 / 20270228
Source-listed ingredients
- NEOMYCIN SULFATE — 3.5 mg/g
- POLYMYXIN B SULFATE — 10000 [USP'U]/g
- DEXAMETHASONE — 1 mg/g
These values do not establish equivalence or a dose recommendation.
Packages
- 3.5 g in 1 TUBE (0078-0771-01) · 0078-0771-01
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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