Divalproex sodium
NDC 65862-595, Divalproex sodium, tablet, film coated, extended release, from Aurobindo Pharma Limited.
- Product NDC
- 65862-595
- Status
- Listed
- Labeler
- Aurobindo Pharma Limited
- Dosage form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA202419
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/65862-595 \ -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 |
|---|---|---|
| 65862-595-01 | 65862059501 | 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65862-595-01) |
| 65862-595-05 | 65862059505 | 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65862-595-05) |
| 65862-595-10 | 65862059510 | 10 BLISTER PACK in 1 CARTON (65862-595-10) / 10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK |
Linked data
RxNorm, label and prices
Related lookups
FDA label sections
GET /v1/drugs/labels/6240cee7-6aa8-425c-ba46-f889a640f0faNADAC price for package 65862059501
GET /v1/drugs/nadac/65862059501NADAC price for package 65862059505
GET /v1/drugs/nadac/65862059505
Use it
Look up 65862-595 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/65862-595 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 65862-595. 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.