FdaApplication
ANDA 206932
Identifiers
- fda_app_no: ANDA206932
Properties
| Property | Value |
|---|---|
| applicant_name | ABHAI LLC |
| application_type | ANDA |
| approval_date | 2017-05-11 |
Products (3)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| METHYLPHENIDATE HYDROCHLORIDE | METHYLPHENIDATE HYDROCHLORIDE | 5MG | TABLET;ORAL |
| METHYLPHENIDATE HYDROCHLORIDE | METHYLPHENIDATE HYDROCHLORIDE | 10MG | TABLET;ORAL |
| METHYLPHENIDATE HYDROCHLORIDE | METHYLPHENIDATE HYDROCHLORIDE | 20MG | TABLET;ORAL |
3 products