Orange Book product
DIVALPROEX SODIUM EQ 250MG VALPROIC ACID
Orange Book ANDA 090062 · PHARMOBEDIENT CONSULTING LLC · Discontinued
Key facts
| Proprietary name | DIVALPROEX SODIUM |
|---|---|
| Active ingredients | DIVALPROEX SODIUM |
| Strength | EQ 250MG VALPROIC ACID |
| Dosage form | TABLET, DELAYED RELEASE |
| Route | ORAL |
| Application | ANDA090062 |
| Applicant holder | PHARMOBEDIENT CONSULTING LLC |
| Marketing status | Discontinued |
| Reference listed drug (RLD) | No |
| Reference standard (RS) | No |
| Approval date | Mar 17, 2009 |
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.