FdaApplication
ANDA 074612
Identifiers
- fda_app_no: ANDA074612
Properties
| Property | Value |
|---|---|
| applicant_name | DIFGEN PHARMACEUTICALS LLC |
| application_type | ANDA |
| approval_date | 1997-10-20 |
Products (3)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| NICOTINE | NICOTINE | 21MG/24HR | FILM, EXTENDED RELEASE;TRANSDERMAL |
| NICOTINE | NICOTINE | 14MG/24HR | FILM, EXTENDED RELEASE;TRANSDERMAL |
| NICOTINE | NICOTINE | 7MG/24HR | FILM, EXTENDED RELEASE;TRANSDERMAL |
3 products