Divalproex Sodium Delayed-release Capsules

SPL v9

SPL

SPL Set ID b0f33792-dd96-40cc-a28e-acdcdca2f4b8

Route

ORAL

Published

Effective Date 2023-09-21

Document Type 34391-3 HUMAN PRESCRIPTION DRUG LABEL

Drug Facts

Composition & Product

Active Ingredients

Valproic Acid (125 mg)

Inactive Ingredients

Alcohol Ammonia Butyl Alcohol Cellulose, Microcrystalline Fd&c Blue No. 1 Ferrosoferric Oxide Gelatin Hypromelloses Isopropyl Alcohol Methacrylic Acid Potassium Hydroxide Propylene Glycol Shellac Silicon Dioxide Sodium Lauryl Sulfate Talc Titanium Dioxide Triethyl Citrate Water

Identifiers & Packaging

Pill Appearance

Imprint: ZA66;125mg Shape: capsule Color: blue Color: white Size: 22 mm Score: 1

Marketing Status

ANDA Active Since 2009-01-27

Description

NDC 65841-639-01 in bottle of 100 Capsules Divalproex sodium delayed-release capsules, USP (sprinkle) Rx only 100 capsules

Medication Information

Description

NDC 65841-639-01 in bottle of 100 Capsules Divalproex sodium delayed-release capsules, USP (sprinkle) Rx only 100 capsules

Package Label.principal Display Panel

NDC 65841-639-01 in bottle of 100 Capsules

Divalproex sodium delayed-release capsules, USP (sprinkle)

Rx only

100 capsules

Structured Label Content

Package Label.principal Display Panel (PACKAGE LABEL.PRINCIPAL DISPLAY PANEL)

NDC 65841-639-01 in bottle of 100 Capsules

Divalproex sodium delayed-release capsules, USP (sprinkle)

Rx only

100 capsules

Advanced Ingredient Data

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Raw Label Data

All Sections (JSON)

{"PACKAGE LABEL.PRINCIPAL DISPLAY PANEL": "NDC 65841-639-01 in bottle of 100 Capsules Divalproex sodium delayed-release capsules, USP (sprinkle) Rx only 100 capsules"}

Additional Information

Back to search View SPL set listing Open on DailyMed ↗

Source: dailymed · Ingested: 2026-02-15T11:43:58.070126 · Updated: 2026-03-14T22:18:18.443233