Divalproex sodium
NDC 71610-205, Divalproex sodium, tablet, film coated, extended release, from Aphena Pharma Solutions - Tennessee, LLC.
- Product NDC
- 71610-205
- 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/71610-205 \ -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 |
|---|---|---|
| 71610-205-30 | 71610020530 | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71610-205-30) |
| 71610-205-53 | 71610020553 | 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71610-205-53) |
| 71610-205-60 | 71610020560 | 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71610-205-60) |
| 71610-205-70 | 71610020570 | 120 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71610-205-70) |
| 71610-205-80 | 71610020580 | 180 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71610-205-80) |
Linked data
RxNorm, label and prices
Related lookups
FDA label sections
GET /v1/drugs/labels/177e34e9-f74d-42aa-8e3c-5fb4f41c2322
Use it
Look up 71610-205 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/71610-205 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 71610-205. 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.