FDA
Neo-Delta-Cortef
The FDA lists this product in 3 strengths and forms.
Composition
- Active ingredients
- NEOMYCIN SULFATE EQ 3.5MG BASE/GM; PREDNISOLONE ACETATE 0.25%
Strengths and forms
The FDA lists each strength of a product separately; these pages share one label.
- NEOMYCIN SULFATE EQ 3.5MG BASE/ML; PREDNISOLONE ACETATE 0.25% · Suspension/dropsANDA061037-001 · Discontinued
- NEOMYCIN SULFATE EQ 3.5MG BASE/GM; PREDNISOLONE ACETATE 0.5% · OintmentANDA061039-001 · Discontinued
- NEOMYCIN SULFATE EQ 3.5MG BASE/GM; PREDNISOLONE ACETATE 0.25% · OintmentThis page
Official product information
Drugs@FDA lists the approved labels, letters and reviews for application ANDA061039.
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
- Neo-Delta-Cortef
- Active substance
- neomycin sulfate
- Route
- Eye
- Dosage form
- Ointment
- Applicant
- Pharmacia and Upjohn
- Status
- Discontinued
- Application
- ANDA061039-002



