FdaApplication
ANDA 218350
Identifiers
- fda_app_no: ANDA218350
Properties
| Property | Value |
|---|---|
| applicant_name | DR REDDYS LABORATORIES LTD |
| application_type | ANDA |
| approval_date | 2025-11-19 |
Products (3)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| NILOTINIB HYDROCHLORIDE | NILOTINIB HYDROCHLORIDE | EQ 150MG BASE | CAPSULE;ORAL |
| NILOTINIB HYDROCHLORIDE | NILOTINIB HYDROCHLORIDE | EQ 50MG BASE | CAPSULE;ORAL |
| NILOTINIB HYDROCHLORIDE | NILOTINIB HYDROCHLORIDE | EQ 200MG BASE | CAPSULE;ORAL |
3 products