Divalproex Sodium Tablet, Delayed Release

What This Divalproex Shortage Record Means

The FDA Drug Shortages database lists this record for Divalproex Sodium Tablet, Delayed Release (brand: DIVALPROEX SODIUM) from Upsher-Smith Laboratories, LLC with a current status of To Be Discontinued. The affected dosage form is Tablet, presented as Divalproex Sodium, Tablet, Delayed Release, 250 mg (NDC 0832-7123-01). Shortages are tracked at the manufacturer and presentation level — other manufacturers or formulations of the same generic may remain available, which is why pharmacists often can source a working substitute even when one record is flagged.

This shortage was first reported on Apr 28, 2025 and was last updated Apr 28, 2025. The FDA cites the following reason: Discontinuation of manufacture of drug based on business decision. There are 6 other current records in this database covering the same generic, which gives a fuller picture of how disruption is playing out across manufacturers and dosage forms.

A shortage listing is a supply-side signal, not a patient-level instruction. Access can vary dramatically by pharmacy, region, hospital system, and insurance formulary — local pharmacists have real-time visibility that a national database cannot provide. Therapeutic substitutes often exist in the same class, but switching decisions belong with your prescriber, who weighs efficacy, dosing conversion, interaction profile, and personal history. This page summarizes public FDA data for educational reference only and is not medical advice. If your medication is affected, contact your pharmacist and prescriber to plan an appropriate response.