FdaApplication
ANDA 215624
Identifiers
- fda_app_no: ANDA215624
Properties
| Property | Value |
|---|---|
| applicant_name | APOTEX INC |
| application_type | ANDA |
| approval_date | 2021-11-26 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| ATROPINE SULFATE | ATROPINE SULFATE | 1% | SOLUTION/DROPS;OPHTHALMIC |
1 product