FdaApplication
NDA 020874
Identifiers
- fda_app_no: NDA020874
Properties
| Property | Value |
|---|---|
| applicant_name | PHARMACIA AND UPJOHN CO |
| application_type | NDA |
| approval_date | 2000-10-05 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| LUNELLE | ESTRADIOL CYPIONATE; MEDROXYPROGESTERONE ACETATE | 5MG/0.5ML;25MG/0.5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | INJECTABLE;INTRAMUSCULAR |
1 product