FdaApplication
ANDA 218722
Identifiers
- fda_app_no: ANDA218722
Properties
| Property | Value |
|---|---|
| applicant_name | ALKEM LABORATORIES LTD |
| application_type | ANDA |
| approval_date | 2026-06-17 |
Products (2)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| SOLRIAMFETOL HYDROCHLORIDE | SOLRIAMFETOL HYDROCHLORIDE | EQ 150MG BASE | TABLET;ORAL |
| SOLRIAMFETOL HYDROCHLORIDE | SOLRIAMFETOL HYDROCHLORIDE | EQ 75MG BASE | TABLET;ORAL |
2 products