FdaApplication
ANDA 205937
Identifiers
- fda_app_no: ANDA205937
Properties
| Property | Value |
|---|---|
| applicant_name | SCIEGEN PHARMACEUTICALS INC |
| application_type | ANDA |
| approval_date | 2015-12-09 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| CYCLOPENTOLATE HYDROCHLORIDE | CYCLOPENTOLATE HYDROCHLORIDE | 0.5% | SOLUTION/DROPS;OPHTHALMIC |
1 product