FdaApplication
ANDA 072130
Identifiers
- fda_app_no: ANDA072130
Properties
| Property | Value |
|---|---|
| applicant_name | AMERICAN THERAPEUTICS INC |
| application_type | ANDA |
| approval_date | 1988-01-14 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| MAPROTILINE HYDROCHLORIDE | MAPROTILINE HYDROCHLORIDE | 50MG | TABLET;ORAL |
1 product