United States · FDA National Drug Code directory
VALPROIC ACID
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 0904-7620_3aea592e-0fb0-4853-83d1-41b2d13c5302
- Product NDC
- 0904-7620
- Form
- SOLUTION
- Composition / generic term
- VALPROIC ACID
- Labeler
- Major Pharmaceuticals
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20260803
- Source listing expiry
- 20271231
Source-listed ingredients
- VALPROIC ACID — 250 mg/5mL
These values do not establish equivalence or a dose recommendation.
Packages
- 10 TRAY in 1 CASE (0904-7620-70) / 10 CUP, UNIT-DOSE in 1 TRAY / 5 mL in 1 CUP, UNIT-DOSE (0904-7620-41) · 0904-7620-70
- 4 TRAY in 1 CASE (0904-7620-94) / 10 CUP, UNIT-DOSE in 1 TRAY / 5 mL in 1 CUP, UNIT-DOSE (0904-7620-41) · 0904-7620-94
Source and coverage
Open FDA National Drug Code directory →
Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
Browse United States records →