FdaApplication
ANDA 209757
Identifiers
- fda_app_no: ANDA209757
Properties
| Property | Value |
|---|---|
| applicant_name | XIAMEN LP PHARMACUETICAL CO LTD |
| application_type | ANDA |
| approval_date | 2017-11-20 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| CLONIDINE HYDROCHLORIDE | CLONIDINE HYDROCHLORIDE | 0.1MG | TABLET, EXTENDED RELEASE;ORAL |
1 product