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
- 0116-4021_4459a233-1fe1-41dc-e063-6394a90a5ab4
- Product NDC
- 0116-4021
- Form
- SOLUTION
- Composition / generic term
- Valproic Acid
- Labeler
- Xttrium Laboratories Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 19860701
- 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 (0116-4021-11) / 10 CUP, UNIT-DOSE in 1 TRAY / 10 mL in 1 CUP, UNIT-DOSE (0116-4021-10) · 0116-4021-11
- 473 mL in 1 BOTTLE, PLASTIC (0116-4021-16) · 0116-4021-16
- 4 TRAY in 1 CASE (0116-4021-40) / 10 CUP, UNIT-DOSE in 1 TRAY / 5 mL in 1 CUP, UNIT-DOSE (0116-4021-05) · 0116-4021-40
- 10 TRAY in 1 CASE (0116-4021-41) / 10 CUP, UNIT-DOSE in 1 TRAY / 5 mL in 1 CUP, UNIT-DOSE (0116-4021-05) · 0116-4021-41
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 →