FdaApplication
NDA 022372
Identifiers
- fda_app_no: NDA022372
Properties
| Property | Value |
|---|---|
| applicant_name | AZURITY PHARMACEUTICALS INC |
| application_type | NDA |
| approval_date | 2010-08-05 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| SUPREP BOWEL PREP KIT | MAGNESIUM SULFATE; POTASSIUM SULFATE; SODIUM SULFATE | 1.6GM/BOT;3.13GM/BOT;17.5GM/BOT | SOLUTION;ORAL |
1 product