FDA
Divalproex Sodium
The FDA lists this product in 60 strengths and forms.
Composition
- Active ingredients
- DIVALPROEX SODIUM EQ 125MG VALPROIC ACID
Strengths and forms
The FDA lists each strength of a product separately; these pages share one label.
- DIVALPROEX SODIUM EQ 500MG VALPROIC ACID · Tablet, extended releaseANDA078239-002 · Prescription
- DIVALPROEX SODIUM EQ 250MG VALPROIC ACID · Tablet, extended releaseANDA078239-001 · Prescription
- DIVALPROEX SODIUM EQ 500MG VALPROIC ACID · Tablet, delayed releaseANDA077254-003 · Discontinued
- DIVALPROEX SODIUM EQ 125MG VALPROIC ACID · Tablet, delayed releaseANDA077254-001 · Discontinued
- DIVALPROEX SODIUM EQ 250MG VALPROIC ACID · Tablet, delayed releaseANDA077254-002 · Discontinued
- DIVALPROEX SODIUM EQ 500MG VALPROIC ACID · Tablet, delayed releaseANDA078790-003 · Discontinued
- DIVALPROEX SODIUM EQ 125MG VALPROIC ACID · Tablet, delayed releaseANDA078790-001 · Discontinued
- DIVALPROEX SODIUM EQ 250MG VALPROIC ACID · Tablet, delayed releaseANDA078790-002 · Discontinued
- DIVALPROEX SODIUM EQ 125MG VALPROIC ACID · Capsule, delayed rel pelletsThis page
- DIVALPROEX SODIUM EQ 125MG VALPROIC ACID · Capsule, delayed rel pelletsANDA213181-001 · Prescription
At a glance
- Brand name
- Divalproex Sodium
- Route
- Oral
- Dosage form
- Capsule, delayed rel pellets
- Applicant
- Rising
- Status
- Discontinued
- FDA approval
- 28 Mar 2011
- Application
- ANDA090407-001
- RxCUI
- 266856