FdaApplication
ANDA 070755
Identifiers
- fda_app_no: ANDA070755
Properties
| Property | Value |
|---|---|
| applicant_name | PAI HOLDINGS LLC DBA PHARMACEUTICAL ASSOCIATES INC |
| application_type | ANDA |
| approval_date | 1986-05-21 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| LITHIUM CITRATE | LITHIUM CITRATE | EQ 300MG CARBONATE/5ML | SYRUP;ORAL |
1 product