FdaApplication
ANDA 087866
Identifiers
- fda_app_no: ANDA087866
Properties
| Property | Value |
|---|---|
| applicant_name | WATSON LABORATORIES INC |
| application_type | ANDA |
| approval_date | 1983-08-25 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| OXTRIPHYLLINE | OXTRIPHYLLINE | 100MG | TABLET, DELAYED RELEASE;ORAL |
1 product