Divalproex sodium
NDC 70518-3477, Divalproex sodium, tablet, extended release, from REMEDYREPACK INC..
- Product NDC
- 70518-3477
- Status
- Listed
- Labeler
- REMEDYREPACK INC.
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA209286
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/70518-3477 \ -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 |
|---|---|---|
| 70518-3477-0 | 70518347700 | 30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (70518-3477-0) |
| 70518-3477-1 | 70518347701 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-3477-1) |
| 70518-3477-3 | 70518347703 | 100 POUCH in 1 BOX (70518-3477-3) / 1 TABLET, EXTENDED RELEASE in 1 POUCH (70518-3477-4) |
| 70518-3477-5 | 70518347705 | 100 POUCH in 1 BOX (70518-3477-5) / 1 TABLET, EXTENDED RELEASE in 1 POUCH (70518-3477-6) |
Linked data
RxNorm, label and prices
Related lookups
FDA label sections
GET /v1/drugs/labels/6af40b06-0a92-454c-9277-80e89de27231
Use it
Look up 70518-3477 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/70518-3477 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 70518-3477. 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.