Orange Book product
DIVALPROEX SODIUM EQ 125MG VALPROIC ACID
Orange Book ANDA 090407 · RISING PHARMA HOLDING INC · Discontinued
Key facts
| Proprietary name | DIVALPROEX SODIUM |
|---|---|
| Active ingredients | DIVALPROEX SODIUM |
| Strength | EQ 125MG VALPROIC ACID |
| Dosage form | CAPSULE, DELAYED REL PELLETS |
| Route | ORAL |
| Application | ANDA090407 |
| Applicant holder | RISING PHARMA HOLDING INC |
| Marketing status | Discontinued |
| Reference listed drug (RLD) | No |
| Reference standard (RS) | No |
| Approval date | Mar 28, 2011 |
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.