Diclofenac Sodium Delayed Release
NDC 70518-2707, Diclofenac Sodium, tablet, delayed release, from REMEDYREPACK INC..
- Product NDC
- 70518-2707
- Status
- Listed
- Labeler
- REMEDYREPACK INC.
- Dosage form
- TABLET, DELAYED RELEASE
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA075185
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/70518-2707 \ -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 |
|---|---|---|
| 70518-2707-3 | 70518270703 | 30 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (70518-2707-3) |
Linked data
RxNorm, label and prices
Related lookups
FDA label sections
GET /v1/drugs/labels/ddd2278b-70be-41ca-8a84-e3fe0f1a1561
Use it
Look up 70518-2707 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/70518-2707 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 70518-2707. 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.