FdaApplication
ANDA 071319
Identifiers
- fda_app_no: ANDA071319
Properties
| Property | Value |
|---|---|
| applicant_name | SUPERPHARM CORP |
| application_type | ANDA |
| approval_date | 1987-01-06 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| PROPOXYPHENE NAPSYLATE AND ACETAMINOPHEN | ACETAMINOPHEN; PROPOXYPHENE NAPSYLATE | 650MG;100MG | TABLET;ORAL |
1 product