FdaApplication
ANDA 210338
Identifiers
- fda_app_no: ANDA210338
Properties
| Property | Value |
|---|---|
| applicant_name | JUBILANT GENERICS LTD |
| application_type | ANDA |
| approval_date | 2018-01-29 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| CLONIDINE HYDROCHLORIDE | CLONIDINE HYDROCHLORIDE | 0.1MG | TABLET, EXTENDED RELEASE;ORAL |
1 product