FdaApplication
ANDA 206431
Identifiers
- fda_app_no: ANDA206431
Properties
| Property | Value |
|---|---|
| applicant_name | TARO PHARMACEUTICAL INDUSTRIES LTD |
| application_type | ANDA |
| approval_date | 2024-03-19 |
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