FdaApplication
ANDA 209941
Identifiers
- fda_app_no: ANDA209941
Properties
| Property | Value |
|---|---|
| applicant_name | PAI HOLDINGS LLC DBA PHARMACEUTICAL ASSOCIATES INC AND DBA PAI PHARMA |
| application_type | ANDA |
| approval_date | 2024-07-15 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| SODIUM SULFATE, POTASSIUM SULFATE AND MAGNESIUM SULFATE | MAGNESIUM SULFATE; POTASSIUM SULFATE; SODIUM SULFATE | 1.6GM/BOT;3.13GM/BOT;17.5GM/BOT | SOLUTION;ORAL |
1 product