Divalproex Sodium
NDC 70518-3055, Divalproex Sodium, tablet, delayed release, from REMEDYREPACK INC..
- Product NDC
- 70518-3055
- Status
- Listed
- Labeler
- REMEDYREPACK INC.
- Dosage form
- TABLET, DELAYED RELEASE
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA090554
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/70518-3055 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- DIVALPROEX SODIUM250 mg/1
Pharmacologic classes
Anti-epileptic Agent [EPC]; Decreased Central Nervous System Disorganized Electrical Activity [PE]; Mood Stabilizer [EPC]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 70518-3055-1 | 70518305501 | 100 POUCH in 1 BOX (70518-3055-1) / 1 TABLET, DELAYED RELEASE in 1 POUCH (70518-3055-2) |
| 70518-3055-3 | 70518305503 | 100 POUCH in 1 BOX (70518-3055-3) / 1 TABLET, DELAYED RELEASE in 1 POUCH (70518-3055-4) |
| 70518-3055-5 | 70518305505 | 60 TABLET, DELAYED RELEASE in 1 BLISTER PACK (70518-3055-5) |
| 70518-3055-6 | 70518305506 | 30 TABLET, DELAYED RELEASE in 1 BLISTER PACK (70518-3055-6) |
| 70518-3055-7 | 70518305507 | 30 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (70518-3055-7) |
Linked data
RxNorm, label and prices
Related lookups
FDA label sections
GET /v1/drugs/labels/5926c3ff-c995-4789-941c-d38aa7db94dc
Use it
Look up 70518-3055 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/70518-3055 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 70518-3055. 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.