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
- 70518-3805_53bf570a-deeb-ede3-e063-6294a90ad4dc
- Product NDC
- 70518-3805
- Form
- SOLUTION
- Composition / generic term
- VALPROIC ACID
- Labeler
- REMEDYREPACK INC.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20230725
- 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, UNIT-DOSE in 1 BOX (70518-3805-0) / 5 mL in 1 CUP, UNIT-DOSE (70518-3805-1) · 70518-3805-0
- 10 CUP, UNIT-DOSE in 1 BOX (70518-3805-2) / 10 mL in 1 CUP, UNIT-DOSE (70518-3805-3) · 70518-3805-2
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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