FdaApplication
ANDA 072319
Identifiers
- fda_app_no: ANDA072319
Properties
| Property | Value |
|---|---|
| applicant_name | GOLDLINE LABORATORIES INC |
| application_type | ANDA |
| approval_date | 1988-12-23 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| GLYCOPREP | POLYETHYLENE GLYCOL 3350; POTASSIUM CHLORIDE; SODIUM BICARBONATE; SODIUM CHLORIDE; SODIUM SULFATE ANHYDROUS | 236GM/BOT;2.97GM/BOT;6.74GM/BOT;5.86GM/BOT;22.74GM/BOT | FOR SUSPENSION;ORAL |
1 product