# MAXITROL

NDC: 66758-070
Generic name: neomycin sulfate, polymyxin b sulfate and dexamethasone
Labeler / Manufacturer: Sandoz Inc
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: OINTMENT
Routes: OPHTHALMIC
Marketing started: 19720117
Marketing ended: 20270531
FDA application: NDA050065

## Active ingredients

- DEXAMETHASONE: 1 mg/g
- NEOMYCIN SULFATE: 3.5 mg/g
- POLYMYXIN B SULFATE: 10000 [USP'U]/g

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"66758-070"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=66758-070
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=5776c435-ac60-49b6-8db1-23a3012b9155