divalproex sodium
NDC 81469-492, divalproex sodium, capsule, coated pellets, from First Nation Group, LLC.
- Product NDC
- 81469-492
- Status
- Listed
- Labeler
- First Nation Group, LLC
- Dosage form
- CAPSULE, COATED PELLETS
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA217358
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/81469-492 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- DIVALPROEX SODIUM125 mg/1
Pharmacologic classes
Anti-epileptic Agent [EPC]; Decreased Central Nervous System Disorganized Electrical Activity [PE]; Mood Stabilizer [EPC]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 81469-492-01 | 81469049201 | 100 CAPSULE, COATED PELLETS in 1 BOTTLE (81469-492-01) |
| 81469-492-10 | 81469049210 | 1000 CAPSULE, COATED PELLETS in 1 BOTTLE (81469-492-10) |
Linked data
RxNorm, label and prices
Related lookups
FDA label sections
GET /v1/drugs/labels/a76f9909-28c9-4eb7-8ffd-ff6222fea079
Use it
Look up 81469-492 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/81469-492 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 81469-492. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.
Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.