FdaApplication
ANDA 085772
Identifiers
- fda_app_no: ANDA085772
Properties
| Property | Value |
|---|---|
| applicant_name | WATSON LABORATORIES INC |
| application_type | ANDA |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| BUTABARBITAL SODIUM | BUTABARBITAL SODIUM | 30MG | TABLET;ORAL |
1 product