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
- 70518-4298_5a97f7d4-db88-0f9e-e063-6294a90ae3f2
- Product NDC
- 70518-4298
- Form
- SOLUTION
- Composition / generic term
- Valproic Acid
- Labeler
- REMEDYREPACK INC.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20250227
- Source listing expiry
- 20271231
Source-listed ingredients
- VALPROIC ACID — 250 mg/5mL
These values do not establish equivalence or a dose recommendation.
Packages
- 10 CUP in 1 BOX (70518-4298-0) / 20 mL in 1 CUP (70518-4298-1) · 70518-4298-0
- 10 CUP in 1 BOX (70518-4298-2) / 10 mL in 1 CUP (70518-4298-3) · 70518-4298-2
- 10 CUP in 1 BOX (70518-4298-4) / 5 mL in 1 CUP (70518-4298-5) · 70518-4298-4
Source and coverage
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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.
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