FdaApplication
ANDA 072330
Identifiers
- fda_app_no: ANDA072330
Properties
| Property | Value |
|---|---|
| applicant_name | PUREPAC PHARMACEUTICAL CO |
| application_type | ANDA |
| approval_date | 1988-08-08 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| CLORAZEPATE DIPOTASSIUM | CLORAZEPATE DIPOTASSIUM | 3.75MG | TABLET;ORAL |
1 product