DEA schedule
Is divalproex a controlled substance?
Federal schedule for divalproex from the FDA NDC directory, checked against the DEA controlled substances list.
Source: FDA NDC Directory file dated 2026-10-22. Publisher page
No. Divalproex is not a federally controlled substance. None of its FDA NDC listings carries a DEA schedule, and divalproex is not on the DEA controlled substances list.
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Schedule check
| Source | What it lists |
|---|---|
| FDA NDC directory | 181 prescription listings from 45 labelers, none with a DEA schedule |
| DEA controlled substances list | divalproex is not on the list |
Divalproex NDC listings
| NDC | Product | Form | Strength | Labeler | DEA schedule |
|---|---|---|---|---|---|
| 0074-6114 | Depakote Sprinkles | capsule | 125 mg/1 | AbbVie Inc. | None |
| 0074-7325 | Depakote | tablet, delayed release | 125 mg/1 | AbbVie Inc. | None |
| 0074-7326 | Depakote | tablet, delayed release | 250 mg/1 | AbbVie Inc. | None |
| 0074-7327 | Depakote | tablet, delayed release | 500 mg/1 | AbbVie Inc. | None |
| 0074-7401 | Depakote ER | tablet, extended release | 250 mg/1 | AbbVie Inc. | None |
| 0074-7402 | Depakote ER | tablet, extended release | 500 mg/1 | AbbVie Inc. | None |
| 0615-8237 | Divalproex sodium | capsule | 125 mg/1 | NCS HealthCare of KY, LLC dba Vangard Labs | None |
| 17856-0109 | divalproex sodium | capsule, coated pellets | 125 mg/1 | ATLANTIC BIOLOGICALS CORP. | None |
| 27241-115 | Divalproex sodium | capsule, coated pellets | 125 mg/1 | Ajanta Pharma USA Inc. | None |
| 55154-4759 | Divalproex Sodium | capsule, coated pellets | 125 mg/1 | Cardinal Health 107, LLC | None |
| 65841-639 | divalproex sodium | capsule, coated pellets | 125 mg/1 | Zydus Lifesciences Limited | None |
| 68084-313 | Divalproex Sodium | capsule, coated pellets | 125 mg/1 | American Health Packaging | None |
| 68382-106 | divalproex sodium | capsule, coated pellets | 125 mg/1 | Zydus Pharmaceuticals USA Inc. | None |
| 70518-1749 | divalproex sodium | capsule, coated pellets | 125 mg/1 | REMEDYREPACK INC. | None |
| 70518-3457 | Divalproex sodium | capsule, coated pellets | 125 mg/1 | REMEDYREPACK INC. | None |
| 70756-447 | divalproex sodium | capsule, coated pellets | 125 mg/1 | Lifestar Pharma LLC | None |
| 81469-492 | divalproex sodium | capsule, coated pellets | 125 mg/1 | First Nation Group, LLC | None |
| 0904-6615 | Divalproex sodium | capsule, delayed release | 125 mg/1 | Major Pharmaceuticals | None |
| 46708-821 | Divalproex sodium | capsule, delayed release | 125 mg/1 | Alembic Pharmaceuticals Limited | None |
| 55111-532 | Divalproex sodium | capsule, delayed release | 125 mg/1 | Dr. Reddy's Laboratories Ltd | None |
| 55154-3552 | Divalproex sodium | capsule, delayed release | 125 mg/1 | Cardinal Health 107, LLC | None |
| 62332-821 | Divalproex sodium | capsule, delayed release | 125 mg/1 | Alembic Pharmaceuticals Inc. | None |
| 72603-260 | Divalproex sodium | capsule, delayed release | 125 mg/1 | NorthStar Rx LLC | None |
| 0615-8586 | divalproex sodium | tablet, delayed release | 125 mg/1 | NCS HealthCare of KY, LLC dba Vangard Labs | None |
| 0832-7122 | Divalproex Sodium | tablet, delayed release | 125 mg/1 | Upsher-Smith Laboratories, LLC | None |
| 29300-138 | Divalproex Sodium | tablet, delayed release | 125 mg/1 | Unichem Pharmaceuticals (USA), Inc. | None |
| 50090-4861 | Divalproex Sodium | tablet, delayed release | 125 mg/1 | A-S Medication Solutions | None |
| 50090-7121 | Divalproex Sodium | tablet, delayed release | 125 mg/1 | A-S Medication Solutions | None |
| 50090-7635 | Divalproex Sodium | tablet, delayed release | 125 mg/1 | A-S Medication Solutions | None |
| 55111-529 | divalproex sodium | tablet, delayed release | 125 mg/1 | Dr.Reddy's Laboratories Limited | None |
| 57237-106 | Divalproex Sodium | tablet, delayed release | 125 mg/1 | Rising Pharma Holdings, Inc. | None |
| 60687-857 | Divalproex Sodium | tablet, delayed release | 125 mg/1 | American Health Packaging | None |
| 62756-796 | Divalproex Sodium | tablet, delayed release | 125 mg/1 | Sun Pharmaceutical Industries, Inc. | None |
| 65862-959 | Divalproex Sodium | tablet, delayed release | 125 mg/1 | Aurobindo Pharma Limited | None |
| 68001-472 | Divalproex Sodium | tablet, delayed release | 125 mg/1 | BluePoint Laboratories | None |
| 68180-265 | Divalproex Sodium | tablet, delayed release | 125 mg/1 | Lupin Pharmaceuticals, Inc. | None |
| 69452-433 | divalproex sodium | tablet, delayed release | 125 mg/1 | Bionpharma Inc. | None |
| 70518-3683 | Divalproex Sodium | tablet, delayed release | 125 mg/1 | REMEDYREPACK INC. | None |
| 0615-8587 | divalproex sodium | tablet, delayed release | 250 mg/1 | NCS HealthCare of KY, LLC dba Vangard Labs | None |
| 0832-7123 | Divalproex Sodium | tablet, delayed release | 250 mg/1 | Upsher-Smith Laboratories, LLC | None |
Showing 40 of 181 listings.
Questions
Is divalproex a controlled substance?
No. Divalproex is not a federally controlled substance. None of its FDA NDC listings carries a DEA schedule, and divalproex is not on the DEA controlled substances list.
Is divalproex a narcotic?
No. Divalproex is not on the DEA controlled substances list, so the DEA does not classify it as a narcotic. Its FDA established pharmacologic class is Anti-epileptic Agent and Mood Stabilizer.
Does this page cover state schedules?
No. This page reports the federal schedule only. Some states schedule drugs on their own; check your state board of pharmacy.
More on Divalproex
- What is Divalproex used for?FDA label uses
- Generic for DepakoteFDA Orange Book
- Generic for Depakote ERFDA Orange Book
- What is Depakote used for?FDA label uses
- Is Depakote a controlled substance?Federal schedule
- Anti-epileptic Agents listFDA drug class
- Mood Stabilizers listFDA drug class
- NDC 0074-6114Divalproex NDC record
- NDC 0074-7325Divalproex NDC record
- NDC 0074-7326Divalproex NDC record