FdaApplication
ANDA 062392
Identifiers
- fda_app_no: ANDA062392
Properties
| Property | Value |
|---|---|
| applicant_name | WATSON LABORATORIES INC |
| application_type | ANDA |
| approval_date | 1983-03-31 |
Products (2)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| DOXYCYCLINE HYCLATE | DOXYCYCLINE HYCLATE | EQ 50MG BASE | TABLET;ORAL |
| DOXYCYCLINE HYCLATE | DOXYCYCLINE HYCLATE | EQ 100MG BASE | TABLET;ORAL |
2 products