Diclofenac Sodium Delayed Release
NDC 85509-1103, Diclofenac Sodium, tablet, delayed release, from PHOENIX RX LLC.
- Product NDC
- 85509-1103
- Status
- Listed
- Labeler
- PHOENIX RX LLC
- 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/85509-1103 \ -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 |
|---|---|---|
| 85509-1103-3 | 85509110303 | 30 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (85509-1103-3) |
| 85509-1103-6 | 85509110306 | 60 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (85509-1103-6) |
| 85509-1103-9 | 85509110309 | 90 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (85509-1103-9) |
Linked data
RxNorm, label and prices
Related lookups
FDA label sections
GET /v1/drugs/labels/41472cca-278b-934b-e063-6294a90aaf5d
Use it
Look up 85509-1103 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/85509-1103 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 85509-1103. 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.