FdaApplication
ANDA 076491
Identifiers
- fda_app_no: ANDA076491
Properties
| Property | Value |
|---|---|
| applicant_name | AUROBINDO PHARMA USA INC |
| application_type | ANDA |
| approval_date | 2004-02-05 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| TRILYTE | POLYETHYLENE GLYCOL 3350; POTASSIUM CHLORIDE; SODIUM BICARBONATE; SODIUM CHLORIDE | 420GM/BOT;1.48GM/BOT;5.72GM/BOT;11.2GM/BOT | FOR SOLUTION;ORAL |
1 product