Divalproex Sodium
NDC 72162-2316, Divalproex Sodium, tablet, delayed release, from Bryant Ranch Prepack.
- Product NDC
- 72162-2316
- Status
- Listed
- Labeler
- Bryant Ranch Prepack
- Dosage form
- TABLET, DELAYED RELEASE
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA078597
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/72162-2316 \ -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 |
|---|---|---|
| 72162-2316-1 | 72162231601 | 100 TABLET, DELAYED RELEASE in 1 BOTTLE (72162-2316-1) |
| 72162-2316-5 | 72162231605 | 500 TABLET, DELAYED RELEASE in 1 BOTTLE (72162-2316-5) |
Linked data
RxNorm, label and prices
Related lookups
FDA label sections
GET /v1/drugs/labels/47412563-ec3e-44fd-9f3f-c00b9b09033a
Use it
Look up 72162-2316 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/72162-2316 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 72162-2316. 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.