DIVALPROEX SODIUM
NDC 61919-249, divalproex sodium, tablet, delayed release, from DirectRx.
- Product NDC
- 61919-249
- Status
- Listed
- Labeler
- DirectRx
- Dosage form
- TABLET, DELAYED RELEASE
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA079163
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/61919-249 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- DIVALPROEX SODIUM500 mg/1
Pharmacologic classes
Anti-epileptic Agent [EPC]; Decreased Central Nervous System Disorganized Electrical Activity [PE]; Mood Stabilizer [EPC]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 61919-249-30 | 61919024930 | 30 TABLET, DELAYED RELEASE in 1 BOTTLE (61919-249-30) |
| 61919-249-60 | 61919024960 | 60 TABLET, DELAYED RELEASE in 1 BOTTLE (61919-249-60) |
Linked data
RxNorm, label and prices
Related lookups
FDA label sections
GET /v1/drugs/labels/ce12c7b1-caa9-4224-bb5f-3e20e0281d66
Use it
Look up 61919-249 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/61919-249 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 61919-249. 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.