FdaApplication
NDA 019381
Identifiers
- fda_app_no: NDA019381
Properties
| Property | Value |
|---|---|
| applicant_name | NOVARTIS PHARMACEUTICALS CORP |
| application_type | NDA |
| approval_date | 1986-04-16 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| TEN-K | POTASSIUM CHLORIDE | 10MEQ | TABLET, EXTENDED RELEASE;ORAL |
1 product