FdaApplication
ANDA 070999
Identifiers
- fda_app_no: ANDA070999
Properties
| Property | Value |
|---|---|
| applicant_name | FUTURE PAK LTD |
| application_type | ANDA |
| approval_date | 1987-10-22 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| K+10 | POTASSIUM CHLORIDE | 10MEQ | TABLET, EXTENDED RELEASE;ORAL |
1 product