FdaApplication
ANDA 203298
Identifiers
- fda_app_no: ANDA203298
Properties
| Property | Value |
|---|---|
| applicant_name | LOTUS PHARMACEUTICAL CO LTD NANTOU PLANT |
| application_type | ANDA |
| approval_date | 2016-07-26 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| CALCIUM ACETATE | CALCIUM ACETATE | 667MG | CAPSULE;ORAL |
1 product