Orange Book product
DULOXETINE HYDROCHLORIDE EQ 20MG BASE
Orange Book ANDA 090745 · SUN PHARMACEUTICAL INDUSTRIES LTD · Discontinued
Key facts
| Proprietary name | DULOXETINE HYDROCHLORIDE |
|---|---|
| Active ingredients | DULOXETINE HYDROCHLORIDE |
| Strength | EQ 20MG BASE |
| Dosage form | CAPSULE, DELAYED REL PELLETS |
| Route | ORAL |
| Application | ANDA090745 |
| Applicant holder | SUN PHARMACEUTICAL INDUSTRIES LTD |
| Marketing status | Discontinued |
| Reference listed drug (RLD) | No |
| Reference standard (RS) | No |
| Approval date | Dec 11, 2013 |
At a glance
- 10–99 Marketed products with the same ingredient, strength and form
- 1–9 Products in this application
- No Reference listed drug
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About Orange Book products
The FDA Orange Book lists approved drug products with their therapeutic equivalence (TE) codes, reference listed drugs and marketing status. Products approved before 1982 show an approval date of Jan 1, 1982.