FdaApplication
NDA 020655
Identifiers
- fda_app_no: NDA020655
Properties
| Property | Value |
|---|---|
| applicant_name | ABBVIE INC |
| application_type | NDA |
| approval_date | 1996-12-20 |
Products (4)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| ALORA | ESTRADIOL | 0.075MG/24HR | FILM, EXTENDED RELEASE;TRANSDERMAL |
| ALORA | ESTRADIOL | 0.05MG/24HR | FILM, EXTENDED RELEASE;TRANSDERMAL |
| ALORA | ESTRADIOL | 0.1MG/24HR | FILM, EXTENDED RELEASE;TRANSDERMAL |
| ALORA | ESTRADIOL | 0.025MG/24HR | FILM, EXTENDED RELEASE;TRANSDERMAL |
4 products