FdaApplication
NDA 019561
Identifiers
- fda_app_no: NDA019561
Properties
| Property | Value |
|---|---|
| applicant_name | KV PHARMACEUTICAL CO |
| application_type | NDA |
| approval_date | 1988-08-26 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| MICRO-K LS | POTASSIUM CHLORIDE | 20MEQ/PACKET **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | FOR SUSPENSION, EXTENDED RELEASE;ORAL |
1 product