FdaApplication
NDA 020700
Identifiers
- fda_app_no: NDA020700
Properties
| Property | Value |
|---|---|
| applicant_name | VIATRIS SPECIALTY LLC |
| application_type | NDA |
| approval_date | 1996-11-19 |
Products (4)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| MUSE | ALPROSTADIL | 0.5MG | SUPPOSITORY;URETHRAL |
| MUSE | ALPROSTADIL | 0.25MG | SUPPOSITORY;URETHRAL |
| MUSE | ALPROSTADIL | 0.125MG | SUPPOSITORY;URETHRAL |
| MUSE | ALPROSTADIL | 1MG | SUPPOSITORY;URETHRAL |
4 products