Composition
- Active ingredients
- HYDROCORTISONE 1%; NEOMYCIN SULFATE EQ 3.5MG BASE/ML; POLYMYXIN B SULFATE 10,000 UNITS/ML
Strengths and forms
The FDA lists each strength of a product separately; these pages share one label.
- HYDROCORTISONE 1%; NEOMYCIN SULFATE EQ 3.5MG BASE/ML; POLYMYXIN B SULFATE 10,000 UNITS/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** · Solution/dropsNDA050479-001 · Discontinued
- HYDROCORTISONE 1%; NEOMYCIN SULFATE EQ 3.5MG BASE/ML; POLYMYXIN B SULFATE 10,000 UNITS/ML · Suspension/dropsThis page
Official product information
Drugs@FDA lists the approved labels, letters and reviews for application NDA050169.
Prognia shows this product information for reference and learning. It is not treatment advice and can lag behind the official text. Always check the current product information and local protocols before prescribing.
At a glance
- Brand name
- Cortisporin
- Active substance
- hydrocortisone
- Route
- Eye
- Dosage form
- Suspension/drops
- Applicant
- Monarch Pharms
- Status
- Discontinued
- FDA approval
- 18 Dec 1964
- Application
- NDA050169-001