FdaApplication
NDA 018833
Identifiers
- fda_app_no: NDA018833
Properties
| Property | Value |
|---|---|
| applicant_name | BAYER PHARMACEUTICALS CORP |
| application_type | NDA |
| approval_date | 1985-07-18 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| LITHANE | LITHIUM CARBONATE | 300MG | TABLET;ORAL |
1 product