DICLOFENAC SODIUM
NDC 82868-114, DICLOFENAC SODIUM, tablet, delayed release, from Northwind Health Company, LLC.
- Product NDC
- 82868-114
- Status
- Listed
- Labeler
- Northwind Health Company, LLC
- Dosage form
- TABLET, DELAYED RELEASE
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA075281
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/82868-114 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- DICLOFENAC SODIUM75 mg/1
Pharmacologic classes
Anti-Inflammatory Agents, Non-Steroidal [CS]; Cyclooxygenase Inhibitors [MoA]; Decreased Prostaglandin Production [PE]; Nonsteroidal Anti-inflammatory Drug [EPC]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 82868-114-30 | 82868011430 | 30 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (82868-114-30) |
Linked data
RxNorm, label and prices
Related lookups
FDA label sections
GET /v1/drugs/labels/5990259d-2f90-20d3-e063-6394a90a3d23
Use it
Look up 82868-114 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/82868-114 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 82868-114. 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.