FDA
Cortef Acetate
The FDA lists this product in 3 strengths and forms.
Composition
- Active ingredients
- HYDROCORTISONE ACETATE 2.5% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Strengths and forms
The FDA lists each strength of a product separately; these pages share one label.
- HYDROCORTISONE ACETATE 50MG/ML · InjectableNDA009378-002 · Discontinued
- HYDROCORTISONE ACETATE 1% · OintmentNDA008917-002 · Discontinued
- HYDROCORTISONE ACETATE 2.5% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** · OintmentThis page
Official product information
Drugs@FDA lists the approved labels, letters and reviews for application NDA008917.
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
- Cortef Acetate
- Active substance
- hydrocortisone acetate
- Route
- Topical
- Dosage form
- Ointment
- Applicant
- Pharmacia and Upjohn
- Status
- Discontinued
- FDA approval
- 28 Jul 1953
- Application
- NDA008917-001