FdaApplication
ANDA 090217
Identifiers
- fda_app_no: ANDA090217
Properties
| Property | Value |
|---|---|
| applicant_name | SUN PHARMACEUTICAL INDUSTRIES INC |
| application_type | ANDA |
| approval_date | 2016-01-29 |
Products (3)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| MINOCYCLINE HYDROCHLORIDE | MINOCYCLINE HYDROCHLORIDE | EQ 100MG BASE | TABLET;ORAL |
| MINOCYCLINE HYDROCHLORIDE | MINOCYCLINE HYDROCHLORIDE | EQ 50MG BASE | TABLET;ORAL |
| MINOCYCLINE HYDROCHLORIDE | MINOCYCLINE HYDROCHLORIDE | EQ 75MG BASE | TABLET;ORAL |
3 products