FdaApplication
ANDA 212017
Identifiers
- fda_app_no: ANDA212017
Properties
| Property | Value |
|---|---|
| applicant_name | YICHANG HUMANWELL PHARMACEUTICAL CO LTD |
| application_type | ANDA |
| approval_date | 2019-06-10 |
Products (3)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| NIACIN | NIACIN | 750MG | TABLET, EXTENDED RELEASE;ORAL |
| NIACIN | NIACIN | 500MG | TABLET, EXTENDED RELEASE;ORAL |
| NIACIN | NIACIN | 1GM | TABLET, EXTENDED RELEASE;ORAL |
3 products