Composition
- Active ingredients
- HYDROCORTISONE 1%; NEOMYCIN SULFATE EQ 3.5MG BASE/ML; POLYMYXIN B SULFATE 10,000 UNITS/ML
Official product information
Drugs@FDA lists the approved labels, letters and reviews for application ANDA062822.
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
- Pediotic
- Active substance
- hydrocortisone
- Route
- Ear
- Dosage form
- Suspension/drops
- Applicant
- Monarch Pharms
- Status
- Discontinued
- FDA approval
- 29 Sept 1987
- Application
- ANDA062822-001



