Divalproex sodium
NDC 71610-249, Divalproex sodium, tablet, film coated, extended release, from Aphena Pharma Solutions - Tennessee, LLC.
- Product NDC
- 71610-249
- Status
- Listed
- Labeler
- Aphena Pharma Solutions - Tennessee, LLC
- 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/71610-249 \ -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 |
|---|---|---|
| 71610-249-30 | 71610024930 | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71610-249-30) |
| 71610-249-53 | 71610024953 | 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71610-249-53) |
| 71610-249-60 | 71610024960 | 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71610-249-60) |
| 71610-249-70 | 71610024970 | 120 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71610-249-70) |
| 71610-249-74 | 71610024974 | 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71610-249-74) |
| 71610-249-80 | 71610024980 | 180 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71610-249-80) |
Linked data
RxNorm, label and prices
Related lookups
FDA label sections
GET /v1/drugs/labels/41e32cd5-1393-4ef1-81cb-8e3795e30682
Use it
Look up 71610-249 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/71610-249 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 71610-249. 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.