NDC 0116-4021 – Valproic Acid

Valproic Acid 250 mg/5mL · Solution · Oral

Human Prescription Drug

Product NDC0116-4021

Product details

Brand name
Valproic Acid
Generic name
Valproic Acid
Labeler
Xttrium Laboratories Inc.
Dosage form
Solution
Route
Oral
Marketing category
ANDA · ANDA070868
Marketed since
July 1, 1986
Listing expires
December 31, 2027
Pharmacologic class
Anti-epileptic Agent; Mood Stabilizer

Active ingredients

Uses, dosage, side effects and warnings for Valproic Acid →

Package NDC codes (4)

Package NDCDescriptionSince
0116-4021-1110 TRAY in 1 CASE (0116-4021-11) / 10 CUP, UNIT-DOSE in 1 TRAY / 10 mL in 1 CUP, UNIT-DOSE (0116-4021-10)Jul 29, 2025
0116-4021-16473 mL in 1 BOTTLE, PLASTIC (0116-4021-16)Jul 29, 2025
0116-4021-404 TRAY in 1 CASE (0116-4021-40) / 10 CUP, UNIT-DOSE in 1 TRAY / 5 mL in 1 CUP, UNIT-DOSE (0116-4021-05)Jul 29, 2025
0116-4021-4110 TRAY in 1 CASE (0116-4021-41) / 10 CUP, UNIT-DOSE in 1 TRAY / 5 mL in 1 CUP, UNIT-DOSE (0116-4021-05)Jul 29, 2025

Other Valproic Acid products