Composition
- Active ingredients
- ESTRADIOL CYPIONATE 5MG/0.5ML; MEDROXYPROGESTERONE ACETATE 25MG/0.5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Official product information
Drugs@FDA lists the approved labels, letters and reviews for application NDA020874.
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
- Lunelle
- Active substance
- estradiol cypionate
- Route
- Intramuscular
- Dosage form
- Injectable
- Applicant
- Pharmacia and Upjohn
- Status
- Discontinued
- FDA approval
- 5 Oct 2000
- Application
- NDA020874-001