FdaApplication
NDA 219131
Identifiers
- fda_app_no: NDA219131
Properties
| Property | Value |
|---|---|
| applicant_name | ALMATICA PHARMA LLC |
| application_type | NDA |
| approval_date | 2026-02-27 |
Products (3)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| DULOXETINE HYDROCHLORIDE | DULOXETINE HYDROCHLORIDE | EQ 120MG BASE | CAPSULE, DELAYED REL PELLETS;ORAL |
| DULOXETINE HYDROCHLORIDE | DULOXETINE HYDROCHLORIDE | EQ 90MG BASE | CAPSULE, DELAYED REL PELLETS;ORAL |
| DULOXETINE HYDROCHLORIDE | DULOXETINE HYDROCHLORIDE | EQ 80MG BASE | CAPSULE, DELAYED REL PELLETS;ORAL |
3 products