FdaApplication
NDA 019155
Identifiers
- fda_app_no: NDA019155
Properties
| Property | Value |
|---|---|
| applicant_name | SUN PHARMACEUTICAL INDUSTRIES INC |
| application_type | NDA |
| approval_date | 1985-04-24 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| LAC-HYDRIN | AMMONIUM LACTATE | EQ 12% BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | LOTION;TOPICAL |
1 product