Diclofenac Sodium
NDC 71610-068, Diclofenac Sodium, tablet, delayed release, from Aphena Pharma Solutions - Tennessee, LLC.
- Product NDC
- 71610-068
- Status
- Listed
- Labeler
- Aphena Pharma Solutions - Tennessee, LLC
- Dosage form
- TABLET, DELAYED RELEASE
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA074514
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/71610-068 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- DICLOFENAC SODIUM50 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 |
|---|---|---|
| 71610-068-80 | 71610006880 | 180 TABLET, DELAYED RELEASE in 1 BOTTLE (71610-068-80) |
Linked data
RxNorm, label and prices
Related lookups
FDA label sections
GET /v1/drugs/labels/e4af374a-1281-46af-a0a9-48820db6c947
Use it
Look up 71610-068 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/71610-068 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 71610-068. 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.