Orange Book product
VENLAFAXINE HYDROCHLORIDE EQ 37.5MG BASE
Orange Book ANDA 078517 · PLIVA HRVATSKA DOO · Discontinued
Key facts
| Proprietary name | VENLAFAXINE HYDROCHLORIDE |
|---|---|
| Active ingredients | VENLAFAXINE HYDROCHLORIDE |
| Strength | EQ 37.5MG BASE |
| Dosage form | TABLET |
| Route | ORAL |
| Application | ANDA078517 |
| Applicant holder | PLIVA HRVATSKA DOO |
| Marketing status | Discontinued |
| Reference listed drug (RLD) | No |
| Reference standard (RS) | No |
| Approval date | Jun 13, 2008 |
At a glance
- 1–9 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.